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FDA Inspection
•Southern California Permanente Medical Group Blood Donor Ctr•November 30, 2011

Southern California Permanente Medical Group Blood Donor Ctr – FDA Inspection, Nov 30, 2011

Record Details

This FDA Inspection record concerns Southern California Permanente Medical Group Blood Donor Ctr, with an inspection on November 30, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Southern California Permanente Medical Group Blood Donor Ctr
Inspection Date
November 30, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · ff3d8f6d-6b52-4b79-9e64-9183380b2eec

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
754873
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

4
  1. 21 CFR 606.100(c)Record review prior to release
  2. 21 CFR 600.14(a)(1)Who must report - receiving information
  3. 21 CFR 606.100(b)Written SOPs available for use by personnel
  4. 21 CFR 606.171Biological product deviation report

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Southern California Permanente Medical Group Blood Donor Ctr

4
DateClassificationOfficeProject area
November 29, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 28, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 9, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 23, 2010NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Southern California Permanente Medical Group Blood Donor Ctr
  • FDA Inspection 1224346 - 2023-11-29
  • FDA Inspection 940276 - 2015-08-28
  • FDA Inspection 843882 - 2013-08-09
  • FDA Inspection 668475 - 2010-06-23

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