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U.S. Department of Health and Human Services

About FDA

Number of highest risk products domestic inspections completed in a month

Cumulative FY 2010 Performance Goal Target: 10,206

Dictionary: A high risk firm is a firm that is producing a food product that may present a high potential for harm if consumed when the food has been prepared under inadequate conditions such as improper processing, storage, handing and distribution.. From this high-risk list, ORA creates a workplan of high-risk inspections to complete for the year.

Fiscal Year - 2010

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Cumulative FY 2010 Performance Goal Target: 10,206

TimeMonthly Guideline to Reach Cumulative FY 2010 Performance Goal TargetNumber
Oct 2009679683
Nov 2009679898
Dec 2009679916
Jan 20101,022888
Feb 20101,022873
Mar 20101,0221,175
Apr 20101,022927
May 20101,022966
Jun 20101,0221,368
Jul 2010679850
Aug 2010680947
Sep 2010680896

FY 2010 YTD: 11,401

Cumulative annual highest risk product domestic inspections completed by the end of the month

Cumulative FY 2010 Performance Goal Target: 10,208

Fiscal Year - 2010

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Cumulative FY 2010 Performance Goal Target: 10,208

TimeTargetNumber
Oct 2009N/A683
Nov 2009N/A1,581
Dec 2009N/A2,497
Jan 2010N/A3,385
Feb 2010N/A4,258
Mar 2010N/A5,433
Apr 2010N/A6,360
May 2010N/A7,326
Jun 2010N/A8,694
Jul 2010N/A9,544
Aug 2010N/A10,491
Sep 2010N/A11,387

Cumulative percent of annual highest risk product domestic inspections completed at the end of the month

Fiscal Year - 2010
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TimeTargetCumulative Percent
Oct 2009N/A7
Nov 2009N/A15
Dec 2009N/A24
Jan 2010N/A33
Feb 2010N/A42
Mar 2010N/A53
Apr 2010N/A62
May 2010N/A72
Jun 2010N/A85
Jul 2010N/A94
Aug 2010N/A103
Sep 2010N/A112

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.