# FDA Inspection 640016 - Osseolink USA, LLC - January 08, 2010

Source: https://www.keypedia.com/records/fda_inspections/osseolink-usa-llc/9ab5b88c-0764-4f04-989f-e30855ef0b21
Source feed: FDA_Inspections

> FDA Inspection 640016 for Osseolink USA, LLC on January 08, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 640016
- Company Name: Osseolink USA, LLC
- Inspection Date: 2010-01-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/osseolink-usa-llc/7cc0c014-3768-40d8-be9a-057e07025c29

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