FDA Warning Letter — Asclemed USA Inc.

Case 575542 — FEI 3001452204

The FDA took a Warning Letter action against Asclemed USA Inc. on June 11, 2019 (Torrance, CA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Asclemed USA Inc.
Date
June 11, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Torrance, CA (United States)