FDA Warning Letter — Linda D. Bosserman

Case 190013 — FEI 3008480759

The FDA took a Warning Letter action against Linda D. Bosserman on July 19, 2011 (La Verne, CA). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Linda D. Bosserman
Date
July 19, 2011
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
La Verne, CA (United States)