# FDA Inspection 1021570 - BioMerieux SA - June 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/biomerieux-sa/0af00fba-6de9-4d98-b472-d43a38e13588
Source feed: FDA_Inspections

> FDA Inspection 1021570 for BioMerieux SA on June 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021570
- Company Name: BioMerieux SA
- Inspection Date: 2017-06-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1021570 - 2017-06-22](https://www.keypedia.com/records/fda_inspections/biomerieux-sa/f25d24a0-acdf-4d55-a139-2472d386f5c9)
- [FDA Inspection 699597 - 2010-11-18](https://www.keypedia.com/records/fda_inspections/biomerieux-sa/7da69cad-6290-4530-9197-6ddfe1438eb0)

Company: https://www.keypedia.com/companies/biomerieux-sa/19e2e522-a53f-4616-949c-f07e054c4c9e

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