FDA Warning Letter — Lin, Henry MD

Case 95226 — FEI 3006789341

The FDA took a Warning Letter action against Lin, Henry MD on March 8, 2010 (Albuquerque, NM). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Lin, Henry MD
Date
March 8, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Albuquerque, NM (United States)