FDA Inspection 1236863 — Bionpharma Inc.

Bionpharma Inc. — FEI 3011705836

The FDA completed an inspection of Bionpharma Inc. on September 19, 2024 in Princeton, NJ. 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 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Princeton, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)