# Synthes (USA), LLC – FDA Inspection, Feb 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/synthes-usa-llc/7e1b1d5a-1002-4486-b69f-1584f8dbc7e3
Source feed: FDA_Inspections

> FDA inspection 565017 of Synthes (USA), LLC, February 25, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 565017
- Company Name: Synthes (USA), LLC
- Inspection Date: 2009-02-25
- 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: 3

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- [FDA Inspection 765879 - 2012-02-01](https://www.keypedia.com/records/fda_inspections/synthes-usa-llc/1f129b0a-71c7-4d62-ba27-6c1972cd340e)

Company: https://www.keypedia.com/companies/synthes-usa-llc/bf9137e7-3e57-4dcd-97cf-de0494f0c7cc

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