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FDA Inspection
•Robins, Edwin MD, PS•July 18, 2012

Robins, Edwin MD, PS – FDA Inspection, Jul 18, 2012

Record Details

This FDA Inspection record concerns Robins, Edwin MD, PS, with an inspection on July 18, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Robins, Edwin MD, PS
Inspection Date
July 18, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 0756b8c9-e3b8-4fc5-a645-b5ca0a440bba

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
791248
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

3
  1. 21 CFR 1271.50(a)Determination based on screening and testing
  2. 21 CFR 1271.90(c)Eligibility not required--warning labels
  3. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Robins, Edwin MD, PS

5
DateClassificationOfficeProject area
June 13, 2025Not classifiedSeattle District Office
September 13, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 12, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 24, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 8, 2010VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Robins, Edwin MD, PS
  • FDA Inspection 1273223 - 2025-06-13
  • FDA Inspection 1180602 - 2022-09-13
  • FDA Inspection 1006801 - 2017-04-12
  • FDA Inspection 934244 - 2015-06-24
  • FDA Inspection 660613 - 2010-04-08

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