# Synthes Tuttlingen GmbH – FDA Inspection, Nov 7, 2013

Source: https://www.keypedia.com/records/fda_inspections/synthes-tuttlingen-gmbh/d85fb3f7-620c-4c11-8663-ddf7c9f89d71
Source feed: FDA_Inspections

> FDA inspection 853842 of Synthes Tuttlingen GmbH, November 07, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853842
- Company Name: Synthes Tuttlingen GmbH
- Inspection Date: 2013-11-07
- 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

- [FDA Inspection 1060885 - 2018-08-02](https://www.keypedia.com/records/fda_inspections/synthes-tuttlingen-gmbh/e76912c9-3fd4-4925-8f5b-211a8c9bb83b)

Company: https://www.keypedia.com/companies/synthes-tuttlingen-gmbh/8e5a5146-dec8-4154-a8bf-8533b2602874

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