# FDA Inspection 612912 - Creaspine SAS - July 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/creaspine-sas/681d6540-6dfc-4bdb-89f7-1c2a199250ae
Source feed: FDA_Inspections

> FDA Inspection 612912 for Creaspine SAS on July 30, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 612912
- Company Name: Creaspine SAS
- Inspection Date: 2009-07-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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

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