# Skeletal Kinetics, Llc – FDA Inspection, Oct 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/skeletal-kinetics-llc/8b363db7-75f2-46e8-b09c-8f45e41a45ab
Source feed: FDA_Inspections

> FDA inspection 1067882 of Skeletal Kinetics, Llc, October 05, 2018. Classification: No Action Indicated (NAI). 2 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: 1067882
- Company Name: Skeletal Kinetics, Llc
- Inspection Date: 2018-10-05
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 938737 - 2015-09-23
- FDA Inspection 786264 - 2012-07-09
- [FDA Inspection 630687 - 2009-11-13](https://www.keypedia.com/records/fda_inspections/skeletal-kinetics-llc/9c48e05f-fb78-4101-b47d-ca9ca98aa493)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/skeletal-kinetics-llc/607f6717-d7d5-447b-92d6-cb21fab2092c

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