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FDA Inspection
•Rentschler Biopharma Inc.•December 10, 2025

Rentschler Biopharma Inc. – FDA Inspection, Dec 10, 2025

Record Details

This FDA Inspection record concerns Rentschler Biopharma Inc., with an inspection on December 10, 2025, issued by the New England District Office, covering biologics.

Company
Rentschler Biopharma Inc.
Inspection Date
December 10, 2025
Product Type
Biologics
Office
New England District Office
Person
  • Burnell M. Henry (FDA Associated Person)
View Company Profile

ID · 9a33c509-4352-4da8-a638-1145baeb9d2f

Inspection Facts

Inspection number
1298478
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Rentschler Biopharma Inc.

5
DateClassificationOfficeProject area
January 17, 2025Not classifiedNew England District Office
March 24, 2023Not classifiedNew England District Office
December 13, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 26, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 23, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Rentschler Biopharma Inc.
  • FDA Inspection 1259307 - 2025-01-17
  • FDA Inspection 1202865 - 2023-03-24
  • FDA Inspection 1116307 - 2019-12-13
  • FDA Inspection 1046134 - 2018-03-26
  • FDA Inspection 961189 - 2016-02-23

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