FDA Inspection 1222105 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3003253380

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Nov 6, 2023 in Pasadena, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 6, 2023
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pasadena, CA (United States)

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing
1225221 CFR 1271.60(a)Completion of eligibility determination
1249321 CFR 1271.90(c)Eligibility not required--warning labels

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.