# InaVein LLC – FDA Inspection, Oct 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/inavein-llc/ce9a0f64-5ad7-4cc8-9a65-d2bfae560501
Source feed: FDA_Inspections

> FDA inspection 683601 of InaVein LLC, October 01, 2010. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 683601
- Company Name: InaVein LLC
- Inspection Date: 2010-10-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [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