# Creaspine SAS – FDA Inspection, Oct 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/creaspine-sas/2bee570d-d71a-44e9-84c8-57cf4c587223
Source feed: FDA_Inspections

> FDA inspection 804960 of Creaspine SAS, October 18, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 804960
- Company Name: Creaspine SAS
- Inspection Date: 2012-10-18
- 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: 2

## Related Documents

- [FDA Inspection 749556 - 2011-09-22](https://www.keypedia.com/records/fda_inspections/creaspine-sas/0b3d173f-2d51-4705-9b1f-de1546dd9888)
- FDA Inspection 612912 - 2009-07-30

Company: https://www.keypedia.com/companies/creaspine-sas/911009fc-5589-4053-9773-d05e86be860e

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