FDA Inspection 1181120 — Alnylam Pharmaceuticals, Inc.

Alnylam Pharmaceuticals, Inc. — FEI 3004080452

The FDA completed an inspection of Alnylam Pharmaceuticals, Inc. on September 9, 2022 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
September 9, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cambridge, MA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)