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<classification authority="sudocs">GA 1.13:AIMD-99-51</classification>
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 <subject>Surplus federal property</subject>
 <subject>Internal controls</subject>
 <subject>Financial statement audits</subject>
 <subject>ADP</subject>
 <subject>Data bases</subject>
 <subject>Data integrity</subject>
 <subject>Information resources management</subject>
 <subject>Federal property management</subject>
 <subject>Equipment inventories</subject>
 <subject>Inventory control systems</subject>
 <identifier>FDA Property Management Information System</identifier>
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<titleInfo>
 <title>Financial Management: FDA&apos;s Controls Over Property Have Improved, But Weaknesses Remain</title>
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<abstract>Pursuant to a congressional request, GAO assessed the adequacy and
status of the Food and Drug Administration&apos;s (FDA) planned actions to
correct internal control weaknesses related to property and equipment
identified in prior financial statement audit reports, focusing on
FDA&apos;s: (1) inadequate controls over the physical quantities of property
and equipment and their locations; (2) improper reconciliations between
its general ledger and property subsidiary ledger systems; and (3)
internal controls related to the safeguarding and reporting of automated
data processing (ADP) equipment that is lost, stolen, destroyed, or
surplussed.&lt;p/&gt;GAO noted that: (1) FDA developed an action plan that should correct the
weaknesses identified in the financial audit reports regarding property
and equipment; (2) FDA has made progress in implementing various
actions, but it has not yet resolved some of the reported weaknesses;
(3) according to FDA officials, as of January 21, 1999, 23 of the 41
tasks in the corrective action plan related to property and equipment
had been completed; (4) GAO found 9 of these 23 tasks had not yet fully
achieved their anticipated outcomes; (5) one of these tasks was for
FDA&apos;s management to create and validate a new property database; (6)
while FDA conducted several physical inventories to create this
database, GAO&apos;s testing showed that the database was not accurate; (7)
FDA did not have adequate controls in place to effectively monitor the
loss, theft, or destruction of ADP equipment; (8) FDA procedures for
reporting and recording missing equipment were ineffective, with the
result that information on missing equipment sometimes never reached the
property management database, thus compromising database accuracy and
completeness; (9) the reliability of the database was further hampered
because FDA used the same code to identify lost, stolen, and destroyed
property and thus could not determine individual quantities and values
in each of these categories; (10) this was the case for $10.1 million in
property, including ADP equipment, that FDA reported in 1998 as having
been lost, stolen, or destroyed; (11) for $7.4 million of the $10.1
million, FDA was unable to determine how much represented lost versus
stolen or destroyed property even when it reviewed source documents;
(12) FDA management could not effectively analyze the nature and
severity of problems related to missing equipment and develop related
management strategies to address its risks; (13) FDA was unable to
provide assurance that the proper authorizations were in place before
ADP equipment was designated for surplus and removed from FDA premises;
(14) FDA&apos;s procedures for surplussing equipment called for filing
related paperwork that included the original signatures of the property
management personnel who authorized the surplus; (15) GAO found that in
8 of the 27 cases it reviewed, FDA staff altered the forms used to
designate equipment for surplus; (16) such alterations of required
paperwork seriously compromised the control environment and increased
the risk of theft and inappropriate removal of equipment; and (17) GAO
also found an instance in which a computer donated to a school contained
information that should have been removed before it was donated.</abstract>
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<identifier type="preferred citation">GAO/AIMD-99-51</identifier>
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<note>Letter Report</note>
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 <searchTitle>GAO/AIMD-99-51; Financial Management: FDA&apos;s Controls Over Property Have Improved, But Weaknesses Remain;
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<subject>
 <topic>Surplus federal property</topic>
 <topic>Internal controls</topic>
 <topic>Financial statement audits</topic>
 <topic>ADP</topic>
 <topic>Data bases</topic>
 <topic>Data integrity</topic>
 <topic>Information resources management</topic>
 <topic>Federal property management</topic>
 <topic>Equipment inventories</topic>
 <topic>Inventory control systems</topic>
 <topic>FDA Property Management Information System</topic>
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