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FDA Inspection
•Northern California Community Blood Bank•August 21, 2009

Northern California Community Blood Bank – FDA Inspection, Aug 21, 2009

Record Details

This FDA Inspection record concerns Northern California Community Blood Bank, with an inspection on August 21, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Northern California Community Blood Bank
Inspection Date
August 21, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · daf29ca2-3d59-4bff-b890-68a9a22687f6

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
607252
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

5
  1. 21 CFR 606.160(b)Required records
  2. 21 CFR 1271.320(a)Procedures re complaints
  3. 21 CFR 1271.160(b)(6)Deviations--Investigation, documenting, trending
  4. 21 CFR 606.100(b)(5)Accurate measurement of quantity of blood
  5. 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 Northern California Community Blood Bank

6
DateClassificationOfficeProject area
September 26, 2025Not classifiedSan Francisco District OfficeBlood and Blood Products
December 16, 2022VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 10, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 16, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 19, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Northern California Community Blood Bank
  • FDA Inspection 1254974 - 2025-09-26
  • FDA Inspection 1193351 - 2022-12-16
  • FDA Inspection 1097629 - 2019-07-10
  • FDA Inspection 988718 - 2016-08-16
  • FDA Inspection 861309 - 2013-12-19

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