FDA Inspection 1230050 — Endo USA, Inc.

Endo USA, Inc. — FEI 3001578003

The FDA completed an inspection of Endo USA, Inc. on Aug 15, 2024 in Malvern, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 15, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Malvern, PA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)