# FDA Inspection 1020265 - Biomerieux, Inc. - July 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/biomerieux-inc/33aef11f-5c2d-47e4-bad3-9060ea0afeb8
Source feed: FDA_Inspections

> FDA Inspection 1020265 for Biomerieux, Inc. on July 27, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020265
- Company Name: Biomerieux, Inc.
- Inspection Date: 2017-07-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020265 - 2017-07-27](https://www.keypedia.com/records/fda_inspections/biomerieux-inc/f9e34cc1-7e36-4db0-9de6-60d6c2849418)

Company: https://www.keypedia.com/companies/biomerieux-inc/9cb36940-306d-48c4-af55-3995ed532955

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