# FDA Inspection 810110 - George S. Lipkowitz, M.D. - November 08, 2012

Source: https://www.keypedia.com/records/fda_inspections/george-s-lipkowitz-md/699a3baf-ba04-450e-8c9f-ad144e5c4cd3
Source feed: FDA_Inspections

> FDA Inspection 810110 for George S. Lipkowitz, M.D. on November 08, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 810110
- Company Name: George S. Lipkowitz, M.D.
- Inspection Date: 2012-11-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1053788 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/george-s-lipkowitz-md/67906d10-93aa-4b1c-ac3e-f69e2f99693c)

Company: https://www.keypedia.com/companies/george-s-lipkowitz-md/8e59a098-f71d-46ff-b1fa-36549ca02465

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