# Rex Medical LP, Conshohocken, PA – FDA Inspections

Source: https://www.keypedia.com/companies/rex-medical-lp/85f653ac-86c4-476e-8b9b-fead45d55171

> Inspection records and compliance data for Rex Medical LP in Conshohocken, Pennsylvania. 4 FDA inspections on record, 1 Form 483, last inspected April 19, 2017.

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## Details

- Name: Rex Medical LP
- FEI Number: 3003862657
- Address Line 1: 555 E North Ln Ste 5035
- City: Conshohocken
- State: Pennsylvania
- Zip Code: 19428
- Country Name: United States
- Address: 555 E North Ln Ste 5035, Conshohocken, Pennsylvania 19428, United States
- Country: United States

## Related Documents

- FDA Inspection 1014186 - Rex Medical LP - 2017-04-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2017
- FDA Inspection 1014186 - Rex Medical LP - 2017-04-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2017
- [FDA Inspection 1014186 - Rex Medical LP - 2017-04-19](https://www.keypedia.com/records/fda_inspections/rex-medical-lp/d5ef590d-d2b9-4b5c-9f66-62a1ac734259) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2017
- FDA Inspection 1014186 - Rex Medical LP - 2017-04-19 — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2017
- FDA Inspection 946070 - Rex Medical LP - 2015-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2015
- FDA Inspection 946070 - Rex Medical LP - 2015-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2015
- FDA Inspection 760520 - Rex Medical LP - 2011-12-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2011
- FDA Inspection 760520 - Rex Medical LP - 2011-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2011
- FDA Inspection 614705 - Rex Medical LP - 2009-08-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2009
- FDA Inspection 614705 - Rex Medical LP - 2009-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2009

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