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FDA Inspection
•Huntsville Reproductive Medicine P.C.•July 12, 2018

Huntsville Reproductive Medicine P.C. – FDA Inspection, Jul 12, 2018

Record Details

This FDA Inspection record concerns Huntsville Reproductive Medicine P.C., with an inspection on July 12, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Huntsville Reproductive Medicine P.C.
Inspection Date
July 12, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Christopher J. Adams (Issuing Officer)
View Company Profile

ID · 70493326-6797-4860-a64e-d359c5c502cb

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1058611
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 1271.50(a)Determination based on screening and testing

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Huntsville Reproductive Medicine P.C.

4
DateClassificationOfficeProject area
October 26, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 5, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 22, 2013VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 2, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Huntsville Reproductive Medicine P.C.
  • FDA Inspection 1187473 - 2022-10-26
  • FDA Inspection 983625 - 2016-08-05
  • FDA Inspection 820792 - 2013-02-22
  • FDA Inspection 729969 - 2011-06-02

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