# FDA Inspection 1114129 - Lawrence Groop, DMD - December 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/lawrence-groop-dmd/c526c7ff-9659-41ca-84cb-1763d4f98ab0
Source feed: FDA_Inspections

> FDA Inspection 1114129 for Lawrence Groop, DMD on December 20, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1114129
- Company Name: Lawrence Groop, DMD
- Inspection Date: 2019-12-20
- 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/lawrence-groop-dmd/a5d9c674-99ee-41ad-b871-1d991997283e

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