# FDA Inspection 994815 - David A. Heimansohn, M.D. - November 15, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/david-a-heimansohn-md/84cea93a-1cc1-40aa-a5b2-2eaa6d838df2
Source feed: FDA_Inspections

> FDA Inspection 994815 for David A. Heimansohn, M.D. on November 15, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 994815
- Company Name: David A. Heimansohn, M.D.
- Inspection Date: 2016-11-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1115232 - 2019-12-20](https://www.globalkeysolutions.net/records/fda_inspections/david-a-heimansohn-md/1d263f0b-78e3-4906-afb5-0290243cb88f)

Company: https://www.globalkeysolutions.net/companies/david-a-heimansohn-md/3dbfd2d5-b8c2-49a3-b65a-c60724132b17

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