# FDA Inspection 884639 - Osseolink USA, LLC - June 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/osseolink-usa-llc/46e4b511-e6b5-4281-9356-3260ad1c70ec
Source feed: FDA_Inspections

> FDA Inspection 884639 for Osseolink USA, LLC on June 25, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 884639
- Company Name: Osseolink USA, LLC
- Inspection Date: 2014-06-25
- 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