FDA Inspection 1065622 — Teva Branded Pharmaceutical Products R&D

Teva Branded Pharmaceutical Products R&D — FEI 3004442422

The FDA completed an inspection of Teva Branded Pharmaceutical Products R&D on Aug 24, 2018 in Horsham, 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 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Horsham, PA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)