# LKC Technologies, Inc. – FDA Inspection, Mar 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/lkc-technologies-inc/8fe26ffe-5e01-4be2-94f7-52d01fc9781f
Source feed: FDA_Inspections

> FDA inspection 1046213 of LKC Technologies, Inc., March 29, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046213
- Company Name: LKC Technologies, Inc.
- Inspection Date: 2018-03-29
- 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: 6

## Related Documents

- FDA Inspection 860090 - 2013-12-17
- FDA Inspection 646653 - 2010-03-05

## Related Officers

- [Company Rep](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)
- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

Company: https://www.keypedia.com/companies/lkc-technologies-inc/5721e30b-8087-4450-8f88-bec14f6d71c9

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