# FDA Inspection 552244 - InaVein LLC - December 08, 2008

Source: https://www.keypedia.com/records/fda_inspections/inavein-llc/24b77551-4db9-4d7b-883e-480fda18664f
Source feed: FDA_Inspections

> FDA Inspection 552244 for InaVein LLC on December 08, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 552244
- Company Name: InaVein LLC
- Inspection Date: 2008-12-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 683601 - 2010-10-01](https://www.keypedia.com/records/fda_inspections/inavein-llc/ce9a0f64-5ad7-4cc8-9a65-d2bfae560501)
- [FDA Inspection 683601 - 2010-10-01](https://www.keypedia.com/records/fda_inspections/inavein-llc/3a80ad29-3dd7-4162-bd00-54b0045cb4c8)
- [FDA Inspection 552244 - 2008-12-08](https://www.keypedia.com/records/fda_inspections/inavein-llc/6ce1425c-7540-408f-a46c-df7ab8f635be)

Company: https://www.keypedia.com/companies/inavein-llc/38d24344-1e2c-4b7c-b2ea-a0d23d6854fe

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