# Betacera Inc. – FDA Inspection, Jun 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/betacera-inc/94c3a41e-74b0-4438-a86e-66887a8ff5ce
Source feed: FDA_Inspections

> FDA inspection 1021280 of Betacera Inc., June 29, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021280
- Company Name: Betacera Inc.
- Inspection Date: 2017-06-29
- 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: 0

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/betacera-inc/fefc0cad-bec1-40a6-a7da-8b6e56eab309

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