# KORR Medical Technologies, Inc. – FDA Inspection, Nov 7, 2016

Source: https://www.keypedia.com/records/fda_inspections/korr-medical-technologies-inc/2cb49d36-690a-4b7a-ac73-e651530e1418
Source feed: FDA_Inspections

> FDA inspection 991323 of KORR Medical Technologies, Inc., November 07, 2016. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991323
- Company Name: KORR Medical Technologies, Inc.
- Inspection Date: 2016-11-07
- 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: 8

## Related Documents

- FDA Inspection 1164820 - 2022-03-17
- FDA Inspection 878261 - 2014-05-10
- FDA Inspection 722658 - 2011-05-03

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/korr-medical-technologies-inc/0ff5c8a9-9b3e-4bcc-b8b8-97e4e6b2e80d

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