FDA Warning Letter — Protech Professional Products, Inc.

Case 420411 — FEI 1000137415

The FDA took a Warning Letter action against Protech Professional Products, Inc. on Jul 24, 2014 (Boynton Beach, FL). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Protech Professional Products, Inc.
Date
Jul 24, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Boynton Beach, FL (United States)