# Brijeshwar S. Maini, M.D. – FDA Inspection, Jun 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/brijeshwar-s-maini-md/c238225b-9be0-4ab8-8467-dbd1a36d64e5
Source feed: FDA_Inspections

> FDA inspection 1020607 of Brijeshwar S. Maini, M.D., June 30, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020607
- Company Name: Brijeshwar S. Maini, M.D.
- Inspection Date: 2017-06-30
- 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: 2

## Related Documents

- FDA Inspection 694684 - 2010-09-30
- FDA Inspection 683381 - 2010-09-30

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/ethan-p-stegman/a2bd07b8-1289-4d95-a362-7a95aa6708c9)

Company: https://www.keypedia.com/companies/brijeshwar-s-maini-md/67796020-e2a2-4431-9d8e-9075914ea927

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