# FDA Inspection 1035361 - Laboratoires Urgo - December 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/laboratoires-urgo/3d37079b-f560-4a0e-a884-0044e804649e
Source feed: FDA_Inspections

> FDA Inspection 1035361 for Laboratoires Urgo on December 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035361
- Company Name: Laboratoires Urgo
- Inspection Date: 2017-12-14
- 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 1035361 - 2017-12-14](https://www.keypedia.com/records/fda_inspections/laboratoires-urgo/be937eb9-871a-4539-b30a-f39f5fb904f0)

Company: https://www.keypedia.com/companies/laboratoires-urgo/778edcaf-341c-48fe-939c-c5ddb29b12b8

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