# Synthes (USA) Products LLC, West Chester, PA – FDA Inspections

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

> Inspection records and compliance data for Synthes (USA) Products LLC in West Chester, Pennsylvania. 7 FDA inspections on record, 2 Form 483s, last inspected October 20, 2017.

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## Details

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

## Related Documents

- [FDA Inspection 1029323 - Synthes (USA) Products LLC - 2017-10-20](https://www.keypedia.com/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 — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2017
- [FDA Inspection 1028729 - Synthes (USA) Products LLC - 2017-10-13](https://www.keypedia.com/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 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 13, 2017
- FDA Inspection 1083832 - Synthes (USA) Products LLC - 2017-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2017
- FDA Inspection 695834 - Synthes (USA) Products LLC - 2010-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2010
- FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2009
- FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2009
- [FDA Inspection 583439 - Synthes (USA) Products LLC - 2009-04-27](https://www.keypedia.com/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 585143 - Synthes (USA) Products LLC - 2009-04-20 — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2009

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