# Osseolink USA, LLC – FDA Inspection, Jun 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/osseolink-usa-llc/afbdc3ac-8491-4baa-8fa7-65c515c16341
Source feed: FDA_Inspections

> FDA inspection 884639 of Osseolink USA, LLC, June 25, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 806 and 820. 5 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

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- [FDA Inspection 1099236 - 2019-06-18](https://www.keypedia.com/records/fda_inspections/osseolink-usa-llc/0f9c391b-d8a8-42b1-aed7-31c1fe7fa94d)
- [FDA Inspection 863826 - 2014-01-29](https://www.keypedia.com/records/fda_inspections/osseolink-usa-llc/c25f25be-fc5b-41db-9086-a8c82d1e0583)
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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
