# FDA Inspection 1125672 - OPKO Diagnostics, LLC - July 01, 2020

Source: https://www.keypedia.com/records/fda_inspections/opko-diagnostics-llc/8ab28e5b-f43e-4d53-8cfd-0a9f074e4f24
Source feed: FDA_Inspections

> FDA Inspection 1125672 for OPKO Diagnostics, LLC on July 01, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1125672
- Company Name: OPKO Diagnostics, LLC
- Inspection Date: 2020-07-01
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1043590 - 2018-01-31](https://www.keypedia.com/records/fda_inspections/opko-diagnostics-llc/032db136-f6a4-497c-bee4-9a69971a6612)

Company: https://www.keypedia.com/companies/opko-diagnostics-llc/9c960759-0431-4e97-b345-fd6bd51ea1e9

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