# FDA Inspection 1028338 - Coligne AG - March 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/coligne-ag/84d6cf86-e56f-4de8-b65e-2720899c5ef7
Source feed: FDA_Inspections

> FDA Inspection 1028338 for Coligne AG on March 29, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028338
- Company Name: Coligne AG
- Inspection Date: 2017-03-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1028338 - 2017-03-29](https://www.keypedia.com/records/fda_inspections/coligne-ag/948194f2-26bf-4ffa-965f-99f3bbc11ae8)

Company: https://www.keypedia.com/companies/coligne-ag/9295d5c1-b61a-4339-ac81-df1764d332a6

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