# FDA Inspection 700702 - OPKO Instrumentation, LLC - December 01, 2010

Source: https://www.keypedia.com/records/fda_inspections/opko-instrumentation-llc/664e7bde-8e01-4e98-bf30-8b7a54fe4be0
Source feed: FDA_Inspections

> FDA Inspection 700702 for OPKO Instrumentation, LLC on December 01, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 700702
- Company Name: OPKO Instrumentation, LLC
- Inspection Date: 2010-12-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 700702 - 2010-12-01](https://www.keypedia.com/records/fda_inspections/opko-instrumentation-llc/09c54776-cb7d-4310-9f32-041afefc95a6)

Company: https://www.keypedia.com/companies/opko-instrumentation-llc/e72909eb-5d94-4ea5-949d-22197b5f20c1

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