# FDA Inspection 1031709 - Meridian Bioscience Inc - November 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/meridian-bioscience-inc/a2f4786e-d42f-48c9-88dc-8a4aded17a0d
Source feed: FDA_Inspections

> FDA Inspection 1031709 for Meridian Bioscience Inc on November 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031709
- Company Name: Meridian Bioscience Inc
- Inspection Date: 2017-11-17
- 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 1031709 - 2017-11-17](https://www.keypedia.com/records/fda_inspections/meridian-bioscience-inc/01eb341f-f70d-4ad5-9991-629a51df2c39)
- [FDA Inspection 882891 - 2014-06-12](https://www.keypedia.com/records/fda_inspections/meridian-bioscience-inc/8cb96cc2-5a77-4c69-a501-aace00f4482c)
- [FDA Inspection 825200 - 2013-03-21](https://www.keypedia.com/records/fda_inspections/meridian-bioscience-inc/3d55c53a-e71b-4c5f-8ba8-61f5659845de)
- [FDA Inspection 825200 - 2013-03-21](https://www.keypedia.com/records/fda_inspections/meridian-bioscience-inc/69a1194c-7305-4657-9de9-61bc080e2c50)

Company: https://www.keypedia.com/companies/meridian-bioscience-inc/45d7a36c-d915-439c-93f2-c7995054c1e8

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