# FDA Inspection 1014186 - Rex Medical LP - April 19, 2017

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

> FDA Inspection 1014186 for Rex Medical LP on April 19, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1014186 - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/rex-medical-lp/b8f1aaf4-df66-4e20-b9e6-d1bea9b4a7a8)
- [FDA Inspection 1014186 - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/rex-medical-lp/3c93b374-b287-4116-bf49-2e0bb05f3e25)
- [FDA Inspection 946070 - 2015-10-23](https://www.globalkeysolutions.net/records/fda_inspections/rex-medical-lp/bc5faebb-3e76-4b7b-9c28-c858fc3a18ac)
- [FDA Inspection 946070 - 2015-10-23](https://www.globalkeysolutions.net/records/fda_inspections/rex-medical-lp/ef1c65e2-f43d-4adf-9072-161cd9967428)
- [FDA Inspection 760520 - 2011-12-16](https://www.globalkeysolutions.net/records/fda_inspections/rex-medical-lp/fea3c1bb-fa73-4597-9ecb-25956b595097)

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

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