FDA Warning Letter — Guidewire Technologies, Inc.

Case 97045 — FEI 1221806

The FDA took a Warning Letter action against Guidewire Technologies, Inc. on February 26, 2010 (Salem, NH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Guidewire Technologies, Inc.
Date
February 26, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Salem, NH (United States)