# FDA Inspection 803435 - Massarat Zutshi MD - October 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/massarat-zutshi-md/161c78ff-ee64-47fe-ac9f-9166dcbe63c6
Source feed: FDA_Inspections

> FDA Inspection 803435 for Massarat Zutshi MD on October 17, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803435
- Company Name: Massarat Zutshi MD
- Inspection Date: 2012-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/massarat-zutshi-md/32f00952-3730-4e15-9055-5b1eb9dbb718

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