# FDA Inspection 893683 - MedGo LLC - September 04, 2014

Source: https://www.keypedia.com/records/fda_inspections/medgo-llc/c90f2aa8-3ca2-4354-89ac-99a693718a30
Source feed: FDA_Inspections

> FDA Inspection 893683 for MedGo LLC on September 04, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893683
- Company Name: MedGo LLC
- Inspection Date: 2014-09-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1024184 - 2017-09-06](https://www.keypedia.com/records/fda_inspections/medgo-llc/14d4361b-e958-4478-96fa-46a01ee87da1)
- [FDA Inspection 893683 - 2014-09-04](https://www.keypedia.com/records/fda_inspections/medgo-llc/f93414db-bf14-4de3-80dd-0600fb457e77)
- [FDA Inspection 893683 - 2014-09-04](https://www.keypedia.com/records/fda_inspections/medgo-llc/2973aaba-be22-4cbe-9bf6-e9a605b4816c)

Company: https://www.keypedia.com/companies/medgo-llc/788d60fd-8379-43f5-927d-fc42c8486059

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