FDA Inspection 803870 — Lannett Company, Inc.

Lannett Company, Inc. — FEI 2510865

The FDA completed an inspection of Lannett Company, Inc. on August 17, 2012 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
August 17, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Philadelphia, PA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)