FDA Warning Letter — Family Fertility Center

Case 588805 — FEI 3003926820

The FDA took a Warning Letter action against Family Fertility Center on September 30, 2019 (Houston, TX). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Family Fertility Center
Date
September 30, 2019
Fiscal Year
2019
Product Type
Biologics
Center
CBER
Location
Houston, TX (United States)