FDA Inspection 1159812 — Sarepta Therapeutics, Inc.

Sarepta Therapeutics, Inc. — FEI 3011431238

The FDA completed an inspection of Sarepta Therapeutics, Inc. on December 6, 2021 in Cambridge, MA. 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
December 6, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cambridge, MA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)