# Synthes (USA) Products LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/synthes-usa-products-llc/f18ef1d0-de31-48cb-afdf-ad711cbff58f

> Inspection records and compliance data for Synthes (USA) Products LLC in West Chester, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Synthes (USA) Products LLC
- FEI Number: 3008812560
- City: West Chester
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 1301 Goshen Pkwy
- Zip Code: 19380

## Related Documents

- [FDA Inspection 1029323 - Synthes (USA) Products LLC - 2017-10-20](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/b799b237-fb7a-4ce6-9de1-6c2017acd681) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 20, 2017
- [FDA Inspection 1032557 - Synthes (USA) Products LLC - 2017-10-17](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/9d45bb6f-fb5e-47d2-b1d5-38cf2318dd65) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2017
- [FDA Inspection 1028729 - Synthes (USA) Products LLC - 2017-10-13](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/d8969994-3d91-441a-a963-512c8f7b20cd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 13, 2017
- [FDA Inspection 1028729 - Synthes (USA) Products LLC - 2017-10-13](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/4644d62c-26a6-4c25-8be6-6a141f7d9c1a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 13, 2017
- [FDA Inspection 1083832 - Synthes (USA) Products LLC - 2017-09-25](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/194092d3-1007-4847-8f76-b12e51eec754) — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2017
- [FDA Inspection 695834 - Synthes (USA) Products LLC - 2010-10-29](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/3a49e31d-94b8-491f-a45b-4dd8f1ebb6f1) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2010
- [FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/9d53449f-a2b0-4e98-acdd-03bf68392a21) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2009
- [FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/f3b6282d-7e11-44a8-8b85-df09fd1b98b8) — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2009
- [FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/21de1472-54fc-4a6c-936e-0b4ae7646f7d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2009
- [FDA Inspection 585143 - Synthes (USA) Products LLC - 2009-04-20](https://www.globalkeysolutions.net/records/fda_inspections/synthes-usa-products-llc/7a8b7a00-b04c-4dd6-86d0-25c16ef8d11c) — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2009

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