# David A. Heimansohn, M.D. – FDA Inspection, Nov 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/david-a-heimansohn-md/f66d3c4a-590b-4355-87c0-78d175850087
Source feed: FDA_Inspections

> FDA inspection 994815 of David A. Heimansohn, M.D., November 15, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## 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)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1115232 - 2019-12-20

## Related Officers

- [Company Rep](https://www.keypedia.com/people/melanie-n-daniels/51d7ddf0-f1af-4e42-ba4c-9a18200f42a9)

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

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