# FDA Inspection 1061989 - Bellus Medical - July 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/df9eeed5-3472-4dae-a9de-d2dbf26c3555
Source feed: FDA_Inspections

> FDA Inspection 1061989 for Bellus Medical on July 25, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061989
- Company Name: Bellus Medical
- Inspection Date: 2018-07-25
- 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 1061989 - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/d47786f8-b844-4ad9-8ce5-8e9745bcec74)
- [FDA Inspection 965933 - 2016-03-23](https://www.globalkeysolutions.net/records/fda_inspections/bellus-medical/c2ef5db8-aa99-4210-a86b-1c4ceb9d7f37)

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