# FDA Inspection 999618 - P. Robert Myers MD - January 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/p-robert-myers-md/0ed8a9b5-ad0a-4608-86a8-b602aa967e2c
Source feed: FDA_Inspections

> FDA Inspection 999618 for P. Robert Myers MD on January 19, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 999618
- Company Name: P. Robert Myers MD
- Inspection Date: 2017-01-19
- 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/p-robert-myers-md/d79c96de-f669-4b3c-a5eb-e7e7f71184d0

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