FDA Inspection 1029763 — Houston Assisted Reproductive Technologies, PLLC

Houston Assisted Reproductive Technologies, PLLC — FEI 3004272066

The FDA completed an inspection of Houston Assisted Reproductive Technologies, PLLC on Oct 23, 2017 in Shenandoah, TX. 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 23, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Shenandoah, TX (United States)

Citations

IDCFRDescription
1227721 CFR 1271.75(a)(1)Risk factors, clinical evidence

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