FDA Inspection 1179443 — REDHILL BIOPHARMA INC.

REDHILL BIOPHARMA INC. — FEI 3016555114

The FDA completed an inspection of REDHILL BIOPHARMA INC. on Aug 25, 2022 in Raleigh, NC. 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
Aug 25, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Raleigh, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)