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FDA Inspection 759349 — Ad-Tech Medical Instrument Corporation

Ad-Tech Medical Instrument Corporation — FEI 2183456

The FDA completed an inspection of Ad-Tech Medical Instrument Corporation on January 11, 2012 in Oak Creek, WI. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 11, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Oak Creek, WI (United States)

Facility

Other inspections at this facility

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  • 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))

Recent compliance actions

FDA data resources