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FDA Inspection
•NW Cryobank•July 19, 2012

NW Cryobank – FDA Inspection, Jul 19, 2012

Record Details

This FDA Inspection record concerns NW Cryobank, with an inspection on July 19, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
NW Cryobank
Inspection Date
July 19, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · b4eeb6eb-b1bb-49a4-9f87-dc8372b27217

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
791251
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

4
  1. 21 CFR 1271.55(d)(2)Accurate, indelible, legible
  2. 21 CFR 1271.50(a)Determination based on screening and testing
  3. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
  4. 21 CFR 1271.75(e)Abbreviated procedure

Full citation text and observation details available on the Dashboard.

Other FDA inspections of NW Cryobank

5
DateClassificationOfficeProject area
June 21, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 18, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 26, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 10, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 7, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for NW Cryobank
  • FDA Inspection 1098187 - 2019-06-21
  • FDA Inspection 983198 - 2016-08-18
  • FDA Inspection 885382 - 2014-06-26
  • FDA Inspection 729656 - 2011-06-10
  • FDA Inspection 660108 - 2010-04-07

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