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FDA Inspection
•Munson Medical Center•August 7, 2026

Munson Medical Center – FDA Inspection, Aug 7, 2026

Record Details

This FDA Inspection record concerns Munson Medical Center, with an inspection on August 7, 2026, issued by the Detroit District Office, covering biologics.

Company
Munson Medical Center
Inspection Date
August 7, 2026
Product Type
Biologics
Office
Detroit District Office
Person
  • Irina Gaberman (FDA Associated Person)
View Company Profile

ID · 4c1b3350-16e0-4dbd-9145-6efdbe72dd5a

Inspection Facts

Inspection number
1329942
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
  2. 21 CFR 606.160(a)(1)Person performing, test results, interpretation
  3. 21 CFR 606.160(b)Required records
  4. 21 CFR 610.47(b)(3)Notify MD, Legal Rep, Relative of Trans Recipient[Consignee]

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Munson Medical Center

6
DateClassificationOfficeProject area
August 3, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 31, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 12, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 15, 2014VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 14, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Munson Medical Center
  • FDA Inspection 1217675 - 2023-08-03
  • FDA Inspection 1067648 - 2018-08-31
  • FDA Inspection 981767 - 2016-08-12
  • FDA Inspection 888226 - 2014-07-15
  • FDA Inspection 786617 - 2012-06-14

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