# FDA Inspection 933356 - Prosidyan Inc - June 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/prosidyan-inc/d57513cc-84f0-452a-bd38-c38dce97f9a7
Source feed: FDA_Inspections

> FDA Inspection 933356 for Prosidyan Inc on June 23, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 933356
- Company Name: Prosidyan Inc
- Inspection Date: 2015-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/prosidyan-inc/3835c310-143b-461a-903f-97fcc98449ae

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