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FDA Inspection
•Peyman Saadat MD, Inc.•February 20, 2024

Peyman Saadat MD, Inc. – FDA Inspection, Feb 20, 2024

Record Details

This FDA Inspection record concerns Peyman Saadat MD, Inc., with an inspection on February 20, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Peyman Saadat MD, Inc.
Inspection Date
February 20, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Dylan R. Jock (Issuing Officer)
View Company Profile

ID · e226d855-6e16-4b64-9d28-5ef11a67542a

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1231316
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 1271.265(c)(2)Improperly released for distribution
  2. 21 CFR 1271.55(b)(1)Statement re: certified testing lab

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Peyman Saadat MD, Inc.

4
DateClassificationOfficeProject area
March 21, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 29, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 16, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 23, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Peyman Saadat MD, Inc.
  • FDA Inspection 1045088 - 2018-03-21
  • FDA Inspection 938669 - 2015-07-29
  • FDA Inspection 796642 - 2012-08-16
  • FDA Inspection 731983 - 2011-06-23

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