# FDA Inspection 679620 - VeeZee Inc dba Von Zipper - September 08, 2010

Source: https://www.keypedia.com/records/fda_inspections/veezee-inc-dba-von-zipper/74b5b7fc-0248-4df6-b029-41f6aae3ade6
Source feed: FDA_Inspections

> FDA Inspection 679620 for VeeZee Inc dba Von Zipper on September 08, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 679620
- Company Name: VeeZee Inc dba Von Zipper
- Inspection Date: 2010-09-08
- 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 679620 - 2010-09-08](https://www.keypedia.com/records/fda_inspections/veezee-inc-dba-von-zipper/b761fc85-0651-41f1-ab80-1e4779144a9c)

Company: https://www.keypedia.com/companies/veezee-inc-dba-von-zipper/89e4b746-af7e-4358-bd6f-698fe989e70d

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