# FDA Inspection 1066892 - Kennametal Stellite L.P. - September 26, 2018

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

> FDA Inspection 1066892 for Kennametal Stellite L.P. on September 26, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1066892 - 2018-09-26](https://www.globalkeysolutions.net/records/fda_inspections/kennametal-stellite-lp/6c73cdfa-251d-47b7-8b50-f7a7241c4233)

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

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