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FDA Inspection 1168052 — Ad-Tech Medical Instrument Corporation

Ad-Tech Medical Instrument Corporation — FEI 2183456

The FDA completed an inspection of Ad-Tech Medical Instrument Corporation on April 7, 2022 in Oak Creek, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 7, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Oak Creek, WI (United States)

Facility

Other inspections at this facility

  • 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))
  • 808283 (VAI Mon Nov 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources