# FDA Inspection 676597 - Verticor, Ltd - August 05, 2010

Source: https://www.keypedia.com/records/fda_inspections/verticor-ltd/a5229dd8-d24c-46b3-aea0-7776ff84bbf0
Source feed: FDA_Inspections

> FDA Inspection 676597 for Verticor, Ltd on August 05, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 676597
- Company Name: Verticor, Ltd
- Inspection Date: 2010-08-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 676597 - 2010-08-05](https://www.keypedia.com/records/fda_inspections/verticor-ltd/35ba3992-9769-4864-8ce1-8b423a2f2635)

Company: https://www.keypedia.com/companies/verticor-ltd/43008dbc-0269-4b54-9fe1-9c77ee642556

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