# Koelis SAS – FDA Inspection, Jun 3, 2015

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

> FDA inspection 932184 of Koelis SAS, June 03, 2015. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1060443 - 2018-07-26](https://www.keypedia.com/records/fda_inspections/koelis-sas/982e1149-865f-45e9-9ce8-1d5dc285b604)

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

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