FDA Inspection 1100682 — Acorda Therapeutics, Inc.

Acorda Therapeutics, Inc. — FEI 3002457563

The FDA completed an inspection of Acorda Therapeutics, Inc. on Jul 19, 2019 in Pearl River, NY. 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
Jul 19, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Pearl River, NY (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

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