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FDA Inspection
•California Central Coast IVF laboratory•September 11, 2026

California Central Coast IVF laboratory – FDA Inspection, Sep 11, 2026

Record Details

This FDA Inspection record concerns California Central Coast IVF laboratory, with an inspection on September 11, 2026, issued by the Los Angeles District Office, covering biologics.

Company
California Central Coast IVF laboratory
Inspection Date
September 11, 2026
Product Type
Biologics
Office
Los Angeles District Office
Person
  • Sunitha K. Rajaram (Company Rep)
View Company Profile

ID · 27159220-0f7f-4edc-bb1d-81b5b7adf491

Inspection Facts

Inspection number
1335426
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of California Central Coast IVF laboratory

1
DateClassificationOfficeProject area
March 1, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for California Central Coast IVF laboratory
  • FDA Inspection 1165128 - 2022-03-01

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