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FDA Inspection
•Reproductive Medicine Institute•August 17, 2018

Reproductive Medicine Institute – FDA Inspection, Aug 17, 2018

Record Details

This FDA Inspection record concerns Reproductive Medicine Institute, with an inspection on August 17, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Reproductive Medicine Institute
Inspection Date
August 17, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Amanda B Vega (Issuing Officer)
View Company Profile

ID · d83594bf-b9d2-4028-81e6-9bd4035acefd

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1062789
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 1271.47(a)Design of procedures to ensure compliance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Reproductive Medicine Institute

1
DateClassificationOfficeProject area
August 17, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Reproductive Medicine Institute
  • FDA Inspection 1216323 - 2023-08-17

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