FDA Inspection 1224705 — Westlake IVF, LLC

Westlake IVF, LLC — FEI 3009085684

The FDA completed an inspection of Westlake IVF, LLC on December 11, 2023 in Austin, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2023
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Austin, TX (United States)

Citations

IDCFRDescription
1223021 CFR 1271.50(a)Responsible person to determine, document
1223821 CFR 1271.55(b)(1)Statement re: certified testing lab
1227221 CFR 1271.65(b)(2)Labeled re: biohazard, risks, test results
1227721 CFR 1271.75(a)(1)Risk factors, clinical evidence
1249321 CFR 1271.90(c)Eligibility not required--warning labels