# Sendx Medical Inc – FDA Inspection, Oct 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/sendx-medical-inc/596b746d-d964-478d-bf3c-0a7290ad9c76
Source feed: FDA_Inspections

> FDA inspection 1031157 of Sendx Medical Inc, October 31, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031157
- Company Name: Sendx Medical Inc
- Inspection Date: 2017-10-31
- 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: 0

## Related Documents

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- FDA Inspection 898205 - 2014-09-29
- [FDA Inspection 557428 - 2009-01-20](https://www.keypedia.com/records/fda_inspections/sendx-medical-inc/df27ac09-afbb-4182-90ea-0c8306fcde67)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/scott-k-zika/7f967edd-5151-438b-a0e7-dd1db8a227d1)

Company: https://www.keypedia.com/companies/sendx-medical-inc/a4b04d63-ec4d-46e1-b7ee-54c51181e126

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