FDA Inspection 918197 — Amedra Pharmaceuticals LLC

Amedra Pharmaceuticals LLC — FEI 3009530344

The FDA completed an inspection of Amedra Pharmaceuticals LLC on March 11, 2015 in Horsham, 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
March 11, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Horsham, PA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)