# FDA Inspection 932125 - Barry S. Horowitz, MD - June 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/barry-s-horowitz-md/cb7d65fe-b703-4888-9676-6b492e4befc9
Source feed: FDA_Inspections

> FDA Inspection 932125 for Barry S. Horowitz, MD on June 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 932125
- Company Name: Barry S. Horowitz, MD
- Inspection Date: 2015-06-26
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 991992 - 2016-10-31](https://www.keypedia.com/records/fda_inspections/barry-s-horowitz-md/3f91c574-e79f-410f-ba77-46b676a5a64f)

Company: https://www.keypedia.com/companies/barry-s-horowitz-md/3953fdfe-ad4d-4ca3-8b39-db2f2b3287a1

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