FDA Inspection 1259307 — Rentschler Biopharma Inc.

Rentschler Biopharma Inc. — FEI 3003282293

The FDA completed an inspection of Rentschler Biopharma Inc. on January 17, 2025 in Milford, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 17, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Milford, MA (United States)