# Neal S. Kleiman, M.D. – FDA Inspection, Dec 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/neal-s-kleiman-md/6e7f99b8-b8f2-448f-8a8f-7fa8d00dd62e
Source feed: FDA_Inspections

> FDA inspection 1074202 of Neal S. Kleiman, M.D., December 06, 2018. 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: 1074202
- Company Name: Neal S. Kleiman, M.D.
- Inspection Date: 2018-12-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 856696 - 2013-11-26](https://www.keypedia.com/records/fda_inspections/neal-s-kleiman-md/e4c22842-c6e7-49fd-acd6-746aa6e73a71)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/leighton-k-ngai/39fc01c8-e40a-45d4-910a-068955d16a06)

Company: https://www.keypedia.com/companies/neal-s-kleiman-md/276044d0-46fe-45c7-9b31-acaaa7ed1423

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