# FDA Inspection 892529 - Grossbard Lee, MD - August 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/grossbard-lee-md/24559359-a2e9-413e-8c2b-dd529113b9e4
Source feed: FDA_Inspections

> FDA Inspection 892529 for Grossbard Lee, MD on August 21, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 892529
- Company Name: Grossbard Lee, MD
- Inspection Date: 2014-08-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/grossbard-lee-md/72bd833a-a073-4b88-a5d9-9503ad740490

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