# Minnesota MedTec, Inc. – FDA Inspection, Apr 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/minnesota-medtec-inc/af2382ff-2dde-4700-a3bb-dd15ede250dc
Source feed: FDA_Inspections

> FDA inspection 972365 of Minnesota MedTec, Inc., April 14, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 972365
- Company Name: Minnesota MedTec, Inc.
- Inspection Date: 2016-04-14
- 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: 1

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Company: https://www.keypedia.com/companies/minnesota-medtec-inc/b6b86664-630b-43ed-b06a-4ec4b3dfe8b9

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