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FDA Inspection
•Huntington Reproductive Center Medical Group•March 28, 2023

Huntington Reproductive Center Medical Group – FDA Inspection, Mar 28, 2023

Record Details

This FDA Inspection record concerns Huntington Reproductive Center Medical Group, with an inspection on March 28, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Huntington Reproductive Center Medical Group
Inspection Date
March 28, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Creighton T. Tuzon (Issuing Officer)
View Company Profile

ID · cebf25f4-6a5e-4f06-9f66-75683b4c873e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1201073
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 1271.50(a)Determination based on screening and testing
  2. 21 CFR 1271.55(c)Name and personal info on accompanying records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Huntington Reproductive Center Medical Group

3
DateClassificationOfficeProject area
October 29, 2024VAILos Angeles District OfficeHuman Cellular, Tissue, and Gene Therapies
March 23, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 9, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Huntington Reproductive Center Medical Group
  • FDA Inspection 1253031 - 2024-10-29
  • FDA Inspection 1056321 - 2018-03-23
  • FDA Inspection 941285 - 2015-09-09

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