FDA Inspection 1018745 — Bionpharma Inc.

Bionpharma Inc. — FEI 3011705836

The FDA completed an inspection of Bionpharma Inc. on June 26, 2017 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
June 26, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Princeton, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)