# FDA Inspection 682243 - ConnexMD - September 22, 2010

Source: https://www.keypedia.com/records/fda_inspections/connexmd/c908252c-0c64-4375-97f4-f1c43b2df45b
Source feed: FDA_Inspections

> FDA Inspection 682243 for ConnexMD on September 22, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 682243
- Company Name: ConnexMD
- Inspection Date: 2010-09-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 682243 - 2010-09-22](https://www.keypedia.com/records/fda_inspections/connexmd/aaac4630-9c20-43d6-97b9-8f9b3179c57d)

Company: https://www.keypedia.com/companies/connexmd/8fc31973-0c09-448e-a8ad-3a582d45cc9a

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