FDA Inspection 1065574 — Tennessee Reproductive Medicine

Tennessee Reproductive Medicine — FEI 3007274509

The FDA completed an inspection of Tennessee Reproductive Medicine on Sep 11, 2018 in Chattanooga, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 11, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Chattanooga, TN (United States)

Citations

IDCFRDescription
1222221 CFR 1271.47(a)Design of procedures to ensure compliance
1222921 CFR 1271.50(a)Determination based on screening and testing