# FDA Inspection 1080275 - 1BYONE PRODUCTS INC - December 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/1byone-products-inc/bde79191-fe28-454a-b76d-9bb3e0fd7897
Source feed: FDA_Inspections

> FDA Inspection 1080275 for 1BYONE PRODUCTS INC on December 11, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1080275
- Company Name: 1BYONE PRODUCTS INC
- Inspection Date: 2018-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1080275 - 2018-12-11](https://www.keypedia.com/records/fda_inspections/1byone-products-inc/9954b666-c3f0-4b78-8f60-0af8b900ca4d)

Company: https://www.keypedia.com/companies/1byone-products-inc/997f9e52-8965-41b4-b5dc-eb070d6e2a91

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