Home / Compliance actions / 410052

FDA Warning Letter — Ad-Tech Medical Instrument Corporation

Case 410052 — FEI 2183456

The FDA took a Warning Letter action against Ad-Tech Medical Instrument Corporation on November 14, 2013 (Oak Creek, WI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Ad-Tech Medical Instrument Corporation
Date
November 14, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Oak Creek, WI (United States)

Facility

Recent inspections

  • 1168052 (VAI Thu Apr 07 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1095446 (VAI Thu Jun 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1024308 (VAI Tue Sep 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884179 (NAI Fri Jun 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 831497 (OAI Wed Jun 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Other compliance actions

FDA data resources