FDA Inspection 961189 — Rentschler Biopharma Inc.

Rentschler Biopharma Inc. — FEI 3003282293

The FDA completed an inspection of Rentschler Biopharma Inc. on February 23, 2016 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
February 23, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milford, MA (United States)