# FDA Inspection 708537 - Grossman, Glenn Mark, MD - January 20, 2011

Source: https://www.keypedia.com/records/fda_inspections/grossman-glenn-mark-md/83a7a828-d793-4352-97d1-3d07e7fc3e3c
Source feed: FDA_Inspections

> FDA Inspection 708537 for Grossman, Glenn Mark, MD on January 20, 2011. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 708537
- Company Name: Grossman, Glenn Mark, MD
- Inspection Date: 2011-01-20
- 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/grossman-glenn-mark-md/5043cd7d-0b3f-4af7-bb08-9e29880a6057

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