FDA Inspection 1048356 — Reproductive Institute of South Texas

Reproductive Institute of South Texas — FEI 3004611200

The FDA completed an inspection of Reproductive Institute of South Texas on April 16, 2018 in Mcallen, 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
April 16, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mcallen, TX (United States)

Citations

IDCFRDescription
1221321 CFR 1271.47(a)Testing, screening, donor eligibility procedures
1223721 CFR 1271.55(a)(3)Summary--records used to make determination
1224221 CFR 1271.55(c)Name and personal info on accompanying records
1224721 CFR 1271.55(d)(2)Accurate, indelible, legible
1227721 CFR 1271.75(a)(1)Risk factors, clinical evidence