FDA Inspection 1107590 — Aspire Fertility Institute San Antonio

Aspire Fertility Institute San Antonio — FEI 3006601457

The FDA completed an inspection of Aspire Fertility Institute San Antonio on Oct 3, 2019 in San Antonio, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 3, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Antonio, TX (United States)

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