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FDA Inspection
•M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank•March 30, 2009

M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank – FDA Inspection, Mar 30, 2009

Record Details

This FDA Inspection record concerns M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank, with an inspection on March 30, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank
Inspection Date
March 30, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 5b764163-ea5a-4edd-806e-721f0d13d6e2

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
572494
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.160(a)(1)Legibility and indelibility
  2. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank

7
DateClassificationOfficeProject area
September 6, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 18, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 8, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 22, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 30, 2013VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for M Health Fairview University of Minnesota Medical Center, East Bank-Blood Bank
  • FDA Inspection 1251216 - 2024-09-06
  • FDA Inspection 1071058 - 2018-10-18
  • FDA Inspection 1001549 - 2017-02-08
  • FDA Inspection 909076 - 2014-12-22
  • FDA Inspection 842523 - 2013-07-30

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