# FDA Inspection 960939 - Cellay, Inc - February 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/cellay-inc/e16c2582-ca3d-4510-a917-30cfc78f5142
Source feed: FDA_Inspections

> FDA Inspection 960939 for Cellay, Inc on February 10, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960939
- Company Name: Cellay, Inc
- Inspection Date: 2016-02-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 667333 - 2010-06-18](https://www.keypedia.com/records/fda_inspections/cellay-inc/99ebd2a1-4f70-43c0-a532-87cf05366215)

Company: https://www.keypedia.com/companies/cellay-inc/3c9c4223-93f1-4b1d-81e9-acd28f7a556d

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