# FDA Inspection 1260145 - Keranetics Inc. - February 06, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/keranetics-inc/3cc05174-5b9e-4a7a-bf67-098a50bacf72
Source feed: FDA_Inspections

> FDA Inspection 1260145 for Keranetics Inc. on February 06, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260145
- Company Name: Keranetics Inc.
- Inspection Date: 2025-02-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1260145 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/keranetics-inc/0d32b2fb-c028-40e9-8d4e-55133b2c3cda)
- [FDA Inspection 1260145 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/keranetics-inc/09ddbf6d-7968-4b36-b069-878e44fb2c57)
- [FDA Inspection 1260145 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/keranetics-inc/4d7b7714-5882-4906-b534-0a9552afc107)

Company: https://www.globalkeysolutions.net/companies/keranetics-inc/e81a83f4-9b6e-4578-86db-b1271860314d

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