FDA Warning Letter — Resilience US, Inc.

Case 44298 — FEI 1000305672

The FDA took a Warning Letter action against Resilience US, Inc. on February 27, 2009 (Allston, MA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Resilience US, Inc.
Date
February 27, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Allston, MA (United States)