# CeraSys Incorporated – FDA Inspection, Oct 29, 2008

Source: https://www.keypedia.com/records/fda_inspections/cerasys-incorporated/6268b21a-689b-48b5-9e65-4affcf5a6d7f
Source feed: FDA_Inspections

> FDA inspection 545672 of CeraSys Incorporated, October 29, 2008. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 545672
- Company Name: CeraSys Incorporated
- Inspection Date: 2008-10-29
- 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: 7

## Related Documents

- [FDA Inspection 770865 - 2012-01-17](https://www.keypedia.com/records/fda_inspections/cerasys-incorporated/4335fe16-3861-4781-891a-5b160de27ddc)
- [FDA Inspection 661480 - 2010-05-03](https://www.keypedia.com/records/fda_inspections/cerasys-incorporated/c5fdbbcf-6fa1-4ee9-ba9a-647ea7e2c573)

Company: https://www.keypedia.com/companies/cerasys-incorporated/52c62a4c-c3c6-4da1-b082-d2feec8d68d5

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