# Moximed, Inc. – FDA Inspection, Jul 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/moximed-inc/b1e6d9c4-ab12-43d8-9a88-da5519f9ecd7
Source feed: FDA_Inspections

> FDA inspection 1019036 of Moximed, Inc., July 07, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019036
- Company Name: Moximed, Inc.
- Inspection Date: 2017-07-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1291320 - 2025-10-28](https://www.keypedia.com/records/fda_inspections/moximed-inc/7308b213-05b3-4877-ad47-ac7480bd3022)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/moximed-inc/68a32f9f-4a0f-4769-8dba-27d139a81f5b

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