FDA Inspection 1116307 — Rentschler Biopharma Inc.

Rentschler Biopharma Inc. — FEI 3003282293

The FDA completed an inspection of Rentschler Biopharma Inc. on December 13, 2019 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milford, MA (United States)