FDA Warning Letter — Padtest, LLC

Case 443370 — FEI 3007799036

The FDA took a Warning Letter action against Padtest, LLC on Dec 17, 2014 (Scottsdale, AZ). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Padtest, LLC
Date
Dec 17, 2014
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Scottsdale, AZ (United States)