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FDA Inspection
•Los Angeles IVF Laboratory•October 19, 2018

Los Angeles IVF Laboratory – FDA Inspection, Oct 19, 2018

Record Details

This FDA Inspection record concerns Los Angeles IVF Laboratory, with an inspection on October 19, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Los Angeles IVF Laboratory
Inspection Date
October 19, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Shelley H. Beausoleil (Issuing Officer)
View Company Profile

ID · aa55d14f-5cc4-494e-968f-4a0b033f67a4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1069504
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 1271.47(b)Review and approval of procedures
  2. 21 CFR 1271.55(a)(3)Summary--records used to make determination
  3. 21 CFR 1271.65(b)(2)Labeled re: biohazard, risks, test results

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Los Angeles IVF Laboratory

1
DateClassificationOfficeProject area
December 14, 2023NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Los Angeles IVF Laboratory
  • FDA Inspection 1227419 - 2023-12-14

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