# FDA Inspection 998392 - VasSol, Inc. - November 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/vassol-inc/d7360de8-2baa-494f-a799-32ca1019a282
Source feed: FDA_Inspections

> FDA Inspection 998392 for VasSol, Inc. on November 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998392
- Company Name: VasSol, Inc.
- Inspection Date: 2016-11-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 861805 - 2014-01-09](https://www.keypedia.com/records/fda_inspections/vassol-inc/989df52a-8286-4c74-ad59-8123af096cbd)
- [FDA Inspection 621719 - 2009-10-13](https://www.keypedia.com/records/fda_inspections/vassol-inc/2fdc7afa-4631-450d-a978-5c642b2cfb79)

Company: https://www.keypedia.com/companies/vassol-inc/da8ce77a-796f-4019-9a24-05ce323aa285

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