# FDA Inspection 965933 - Bellus Medical - March 23, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/c2ef5db8-aa99-4210-a86b-1c4ceb9d7f37
Source feed: FDA_Inspections

> FDA Inspection 965933 for Bellus Medical on March 23, 2016. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965933
- Company Name: Bellus Medical
- Inspection Date: 2016-03-23
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1061989 - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/d47786f8-b844-4ad9-8ce5-8e9745bcec74)
- [FDA Inspection 1061989 - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/df9eeed5-3472-4dae-a9de-d2dbf26c3555)

Company: https://www.globalkeysolutions.net/companies/bellus-medical/db504dc4-24ed-4151-9a75-c1a820fa64ad

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