# Neal S. Kleiman, M.D. – FDA Inspection, Nov 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/neal-s-kleiman-md/e4c22842-c6e7-49fd-acd6-746aa6e73a71
Source feed: FDA_Inspections

> FDA inspection 856696 of Neal S. Kleiman, M.D., November 26, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 856696
- Company Name: Neal S. Kleiman, M.D.
- Inspection Date: 2013-11-26
- 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: 3

## Related Documents

- [FDA Inspection 1074202 - 2018-12-06](https://www.keypedia.com/records/fda_inspections/neal-s-kleiman-md/6e7f99b8-b8f2-448f-8a8f-7fa8d00dd62e)

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