FDA Warning Letter — Phoenix Instruments Inc.

Case 346158 — FEI 1000115048

The FDA took a Warning Letter action against Phoenix Instruments Inc. on November 8, 2012 (Lisle, IL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Phoenix Instruments Inc.
Date
November 8, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Lisle, IL (United States)