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 Jan 11, 2012 in Oak Creek, WI. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.