# FDA Inspection 913098 - Manish Mehta, MD - February 06, 2015

Source: https://www.keypedia.com/records/fda_inspections/manish-mehta-md/9d24da67-f8d5-48cd-af40-685aa494332e
Source feed: FDA_Inspections

> FDA Inspection 913098 for Manish Mehta, MD on February 06, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 913098
- Company Name: Manish Mehta, MD
- Inspection Date: 2015-02-06
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 792362 - 2012-07-09](https://www.keypedia.com/records/fda_inspections/manish-mehta-md/153efa12-0099-4990-9db1-5b51f1f51673)
- [FDA Inspection 787172 - 2012-06-13](https://www.keypedia.com/records/fda_inspections/manish-mehta-md/bc910349-8bcd-44ae-a34f-d92728607a1d)
- [FDA Inspection 750025 - 2011-10-24](https://www.keypedia.com/records/fda_inspections/manish-mehta-md/1ba4faa4-0267-484b-8cd0-26466beb1039)

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
