# Ad-Tech Medical Instrument Corporation – FDA Inspection, Jun 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/209e1bb5-6707-486a-99fe-1e53d5c6fc76
Source feed: FDA_Inspections

> FDA inspection 1095446 of Ad-Tech Medical Instrument Corporation, June 27, 2019. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803 and 820. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095446
- Company Name: Ad-Tech Medical Instrument Corporation
- Inspection Date: 2019-06-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Documents

- FDA Inspection 1168052 - 2022-04-07
- [FDA Inspection 1024308 - 2017-09-05](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/c249c15a-d18f-47a2-82b0-9d3112623b73)
- FDA Inspection 884179 - 2014-06-20
- [FDA Inspection 831497 - 2013-06-05](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/d5b8a0cf-8416-445a-bd5f-d046f3069d01)
- [FDA Inspection 808283 - 2012-11-26](https://www.keypedia.com/records/fda_inspections/ad-tech-medical-instrument-corporation/37c56fe8-5d36-4c53-9c0a-4973427391f3)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michelle-j-glembin/e58f4652-d09f-41a7-941d-335c7b5338ad)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7