FDA Inspection 1018610 — Lannett Company, Inc.

Lannett Company, Inc. — FEI 2510865

The FDA completed an inspection of Lannett Company, Inc. on June 22, 2017 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Philadelphia, PA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)