# Ad-Tech Medical Instrument Corporation, Oak Creek, WI – FDA Inspections

Source: https://www.keypedia.com/companies/ad-tech-medical-instrument-corporation/c1ea8550-2f68-45aa-9ec5-c82ec299b425

> Inspection records and compliance data for Ad-Tech Medical Instrument Corporation in Oak Creek, Wisconsin. 8 FDA inspections on record (2 OAI), 2 Form 483s, 2 warning letters, last inspected April 07, 2022.

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## Details

- Name: Ad-Tech Medical Instrument Corporation
- FEI Number: 2183456
- Address Line 1: 400 W Oakview Pkwy
- City: Oak Creek
- State: Wisconsin
- Zip Code: 53154
- Country Name: United States
- Address: 400 W Oakview Pkwy, Oak Creek, Wisconsin 53154, United States
- Country: United States

## Related Documents

- FDA Inspection 1168052 - Ad-Tech Medical Instrument Corporation - 2022-04-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2022
- FDA Inspection 1168052 - Ad-Tech Medical Instrument Corporation - 2022-04-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2022
- [FDA Inspection 1095446 - Ad-Tech Medical Instrument Corporation - 2019-06-27](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/209e1bb5-6707-486a-99fe-1e53d5c6fc76) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 27, 2019
- FDA Inspection 1024308 - Ad-Tech Medical Instrument Corporation - 2017-09-05 — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2017
- [FDA Inspection 1024308 - Ad-Tech Medical Instrument Corporation - 2017-09-05](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/c249c15a-d18f-47a2-82b0-9d3112623b73) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 5, 2017
- FDA Inspection 884179 - Ad-Tech Medical Instrument Corporation - 2014-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2014
- [WARNING_LETTER - Ad-Tech Medical Instrument Corporation - 2013-06-05](https://www.keypedia.com/records/warning_letter/ad-tech-medical-instrument-corporation/a6b644ae-4770-4ff6-9f2d-944bc09768f1) — source: FDA, date: June 5, 2013
- FDA Inspection 831497 - Ad-Tech Medical Instrument Corporation - 2013-06-05 — classification: Official Action Indicated (OAI), source: FDA, date: June 5, 2013
- [FDA Inspection 831497 - Ad-Tech Medical Instrument Corporation - 2013-06-05](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/d5b8a0cf-8416-445a-bd5f-d046f3069d01) — classification: Official Action Indicated (OAI), source: FDA, date: June 5, 2013
- [FDA Inspection 808283 - Ad-Tech Medical Instrument Corporation - 2012-11-26](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/37c56fe8-5d36-4c53-9c0a-4973427391f3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 26, 2012
- [WARNING_LETTER - Ad-Tech Medical Instrument Corporation - 2012-01-11](https://www.keypedia.com/records/warning_letter/ad-tech-medical-instrument-corporation/239f0ec5-617b-41f7-b1a5-e92324f3b0ce) — source: FDA, date: January 11, 2012
- FDA Inspection 759349 - Ad-Tech Medical Instrument Corporation - 2012-01-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 11, 2012

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## Related Officers

- [Ms.](https://www.keypedia.com/people/joanne-m-givens/7d6d17bd-5f41-4cdf-8f88-488b560f73f8)
- [Acting Assistant Commissioner](https://www.keypedia.com/people/michael-dutcher/5e9981f8-673f-4a2c-a0b5-dd5e8e8de1f4)