FDA Warning Letter — ASI Medical, Inc.

Case 370803 — FEI 1000160293

The FDA took a Warning Letter action against ASI Medical, Inc. on Jan 23, 2013 (Englewood, CO). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
ASI Medical, Inc.
Date
Jan 23, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Englewood, CO (United States)