# FDA Inspection 1007275 - Dr. Paul R. Lambert - April 05, 2017

Source: https://www.keypedia.com/records/fda_inspections/dr-paul-r-lambert/b20ce6a8-c14f-49dd-bf03-5301d0c47503
Source feed: FDA_Inspections

> FDA Inspection 1007275 for Dr. Paul R. Lambert on April 05, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007275
- Company Name: Dr. Paul R. Lambert
- Inspection Date: 2017-04-05
- 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/dr-paul-r-lambert/758b428a-d2fc-43ae-9713-81911fe0f4c0

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