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FDA Inspection 803005 — Upsher-Smith Laboratories, LLC

Upsher-Smith Laboratories, LLC — FEI 1719991

The FDA completed an inspection of Upsher-Smith Laboratories, LLC on September 25, 2012 in Denver, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Denver, CO (United States)

Facility

Other inspections at this facility

  • 1109100 (VAI Thu Nov 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1035142 (NAI Tue Oct 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 742842 (VAI Thu Aug 25 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 661821 (VAI Fri Apr 30 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources