# Manish Mehta, MD – FDA Inspection, Oct 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/manish-mehta-md/1ba4faa4-0267-484b-8cd0-26466beb1039
Source feed: FDA_Inspections

> FDA inspection 750025 of Manish Mehta, MD, October 24, 2011. Classification: Official Action Indicated (OAI). 2 citations under 21 CFR parts 50 and 812. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 750025
- Company Name: Manish Mehta, MD
- Inspection Date: 2011-10-24
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 913098 - 2015-02-06
- FDA Inspection 792362 - 2012-07-09
- [FDA Inspection 787172 - 2012-06-13](https://www.keypedia.com/records/fda_inspections/manish-mehta-md/bc910349-8bcd-44ae-a34f-d92728607a1d)

Company: https://www.keypedia.com/companies/manish-mehta-md/7cf9cbea-6a94-4813-948e-58610e9b65f7

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