FDA Inspection 816222 — Aspire Fertility Institute San Antonio

Aspire Fertility Institute San Antonio — FEI 3006601457

The FDA completed an inspection of Aspire Fertility Institute San Antonio on Jan 28, 2013 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
Jan 28, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Antonio, TX (United States)

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