# FDA Inspection 932184 - Koelis SAS - June 03, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/koelis-sas/ef61440e-5baf-46ca-8bf3-b9fbdbac0e69
Source feed: FDA_Inspections

> FDA Inspection 932184 for Koelis SAS on June 03, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 932184
- Company Name: Koelis SAS
- Inspection Date: 2015-06-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 932184 - 2015-06-03](https://www.globalkeysolutions.net/records/fda_inspections/koelis-sas/dc1df799-5991-4141-af30-0d9a419acd4e)

Company: https://www.globalkeysolutions.net/companies/koelis-sas/8c879c96-a073-43c9-9e83-13ae7f5f5c4a

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