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FDA Inspection 987590 — Lannett Company, Inc.

Lannett Company, Inc. — FEI 2510865

The FDA completed an inspection of Lannett Company, Inc. on September 16, 2016 in Philadelphia, PA. 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 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Philadelphia, PA (United States)

Facility

Other inspections at this facility

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  • 1081137 (NAI Fri Jan 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018610 (NAI Thu Jun 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 844132 (VAI Tue Aug 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 803870 (VAI Fri Aug 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources