# Rex Medical LP – FDA Inspection, Apr 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/rex-medical-lp/d5ef590d-d2b9-4b5c-9f66-62a1ac734259
Source feed: FDA_Inspections

> FDA inspection 1014186 of Rex Medical LP, April 19, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014186
- Company Name: Rex Medical LP
- Inspection Date: 2017-04-19
- 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: 2

## Related Documents

- FDA Inspection 946070 - 2015-10-23
- FDA Inspection 760520 - 2011-12-16
- FDA Inspection 614705 - 2009-08-31

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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

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