# FDA Inspection 1099752 - Randy I. Cooper, MD - August 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/randy-i-cooper-md/5ac3475b-524d-44b2-bd79-485483214f73
Source feed: FDA_Inspections

> FDA Inspection 1099752 for Randy I. Cooper, MD on August 14, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099752
- Company Name: Randy I. Cooper, MD
- Inspection Date: 2019-08-14
- 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/randy-i-cooper-md/b600e203-be5c-4b5d-ae5c-ffdca8a28b0f

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