# KMC Systems, Inc. – FDA Inspection, Oct 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/kmc-systems-inc/c639ee0e-36a2-4962-817e-47f6719ed4e6
Source feed: FDA_Inspections

> FDA inspection 1028786 of KMC Systems, Inc., October 05, 2017. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028786
- Company Name: KMC Systems, Inc.
- Inspection Date: 2017-10-05
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1246379 - 2024-04-10
- [FDA Inspection 1155514 - 2021-08-18](https://www.keypedia.com/records/fda_inspections/kmc-systems-inc/511a8ac8-0370-4c19-a03a-364b18766dca)
- FDA Inspection 921815 - 2015-03-11
- FDA Inspection 819147 - 2013-02-20
- FDA Inspection 683609 - 2010-10-01

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/kmc-systems-inc/0e8d51c9-d4ae-42c0-b29b-88d740c57788

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