# FDA Inspection 561290 - OPKO Instrumentation/OTI - January 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/opko-instrumentationoti/9beddc84-b56f-40d8-80bf-ba3686893ff9
Source feed: FDA_Inspections

> FDA Inspection 561290 for OPKO Instrumentation/OTI on January 22, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 561290
- Company Name: OPKO Instrumentation/OTI
- Inspection Date: 2009-01-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/opko-instrumentationoti/c03722ea-6517-49a1-8300-962c61bb2ca8

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