FDA Warning Letter — GeoTec, Inc.

Case 480160 — FEI 1000120768

The FDA took a Warning Letter action against GeoTec, Inc. on September 30, 2015 (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
GeoTec, Inc.
Date
September 30, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Warwick, RI (United States)