FDA Inspection 1210858 — Apellis Pharmaceuticals, Inc.

Apellis Pharmaceuticals, Inc. — FEI 3016603289

The FDA completed an inspection of Apellis Pharmaceuticals, Inc. on July 14, 2023 in Waltham, 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
July 14, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Waltham, MA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)