# FDA Inspection 1019036 - Moximed, Inc. - July 07, 2017

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

> FDA Inspection 1019036 for Moximed, Inc. on July 07, 2017. Classification: Voluntary Action Indicated (VAI).

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

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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