# Kennametal Stellite L.P. – FDA Inspection, Sep 26, 2018

Source: https://www.keypedia.com/records/fda_inspections/kennametal-stellite-lp/8e5cc1ad-868a-482b-9aa7-3df53f4cb8a0
Source feed: FDA_Inspections

> FDA inspection 1066892 of Kennametal Stellite L.P., September 26, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066892
- Company Name: Kennametal Stellite L.P.
- Inspection Date: 2018-09-26
- 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

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/suyang-qin/c32419c5-1b78-4014-9f94-cb7ab17dfe05)

Company: https://www.keypedia.com/companies/kennametal-stellite-lp/3941a5e0-9957-42f2-9d56-698d719e84b7

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