# Synthes (USA) Products LLC – FDA Inspection, Oct 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/synthes-usa-products-llc/b799b237-fb7a-4ce6-9de1-6c2017acd681
Source feed: FDA_Inspections

> FDA inspection 1029323 of Synthes (USA) Products LLC, October 20, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1029323
- Company Name: Synthes (USA) Products LLC
- Inspection Date: 2017-10-20
- 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: 1

## Related Documents

- FDA Inspection 1032557 - 2017-10-17
- [FDA Inspection 1028729 - 2017-10-13](https://www.keypedia.com/records/fda_inspections/synthes-usa-products-llc/d8969994-3d91-441a-a963-512c8f7b20cd)
- FDA Inspection 1083832 - 2017-09-25
- FDA Inspection 695834 - 2010-10-29
- [FDA Inspection 583439 - 2009-04-27](https://www.keypedia.com/records/fda_inspections/synthes-usa-products-llc/f3b6282d-7e11-44a8-8b85-df09fd1b98b8)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)

Company: https://www.keypedia.com/companies/synthes-usa-products-llc/f18ef1d0-de31-48cb-afdf-ad711cbff58f

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