# FDA Inspection 630237 - David R. Liljenquist, M.D. - October 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/david-r-liljenquist-md/47f6c303-31ba-4141-b78e-ce1a16a88745
Source feed: FDA_Inspections

> FDA Inspection 630237 for David R. Liljenquist, M.D. on October 30, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 630237
- Company Name: David R. Liljenquist, M.D.
- Inspection Date: 2009-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1065396 - 2018-08-03](https://www.keypedia.com/records/fda_inspections/david-r-liljenquist-md/17272b20-8748-4c4a-8aac-e1bee23091fb)
- [FDA Inspection 924149 - 2015-04-17](https://www.keypedia.com/records/fda_inspections/david-r-liljenquist-md/771a32df-db96-4af7-a073-de831a28185f)

Company: https://www.keypedia.com/companies/david-r-liljenquist-md/2682f995-b82a-475c-bd50-a18c7e5453a6

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