FDA Warning Letter — Louisville Reproductive Center

Case 533267 — FEI 3005081370

The FDA took a Warning Letter action against Louisville Reproductive Center on August 29, 2017 (Louisville, KY). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Louisville Reproductive Center
Date
August 29, 2017
Fiscal Year
2017
Product Type
Biologics
Center
CBER
Location
Louisville, KY (United States)