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FDA Inspection
•Robins, Edwin MD, PS•April 8, 2010

Robins, Edwin MD, PS – FDA Inspection, Apr 8, 2010

Record Details

This FDA Inspection record concerns Robins, Edwin MD, PS, with an inspection on April 8, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Robins, Edwin MD, PS
Inspection Date
April 8, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · c7015e6b-4e6f-458f-8f18-413d41959db3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
660613
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.47(a)Procedures for all other requirements

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
July 18, 2012VAICenter 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 791248 - 2012-07-18

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