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FDA Inspection
•Rentschler Biopharma Inc.•March 24, 2023

Rentschler Biopharma Inc. – FDA Inspection, Mar 24, 2023

Record Details

This FDA Inspection record concerns Rentschler Biopharma Inc., with an inspection on March 24, 2023, issued by the New England District Office.

Company
Rentschler Biopharma Inc.
Inspection Date
March 24, 2023
Office
New England District Office
People
  • Charles Y. Kuo (Company Rep)
  • Wendy G. Tan
View Company Profile

ID · 677dabb7-4663-4162-b23d-07be45784457

Inspection Facts

Inspection number
1202865
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Rentschler Biopharma Inc.

5
DateClassificationOfficeProject area
December 10, 2025Not classifiedNew England District Office
January 17, 2025Not 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 1298478 - 2025-12-10
  • FDA Inspection 1259307 - 2025-01-17
  • FDA Inspection 1116307 - 2019-12-13
  • FDA Inspection 1046134 - 2018-03-26
  • FDA Inspection 961189 - 2016-02-23

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