# Synthes (USA) Products LLC – FDA Inspection, Apr 20, 2009

Source: https://www.keypedia.com/records/fda_inspections/synthes-usa-products-llc/d95fe0af-c567-4ba1-ba5f-7200d4e52dd7
Source feed: FDA_Inspections

> FDA inspection 585143 of Synthes (USA) Products LLC, April 20, 2009. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 585143
- Company Name: Synthes (USA) Products LLC
- Inspection Date: 2009-04-20
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1029323 - 2017-10-20](https://www.keypedia.com/records/fda_inspections/synthes-usa-products-llc/b799b237-fb7a-4ce6-9de1-6c2017acd681)
- 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
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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