FDA Warning Letter — Criticare Technologies, Inc.

Case 523101 — FEI 3012238587

The FDA took a Warning Letter action against Criticare Technologies, Inc. on April 21, 2017 (Warwick, RI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Criticare Technologies, Inc.
Date
April 21, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Warwick, RI (United States)