# FDA Inspection 805250 - Kevin B Rapeport - October 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/kevin-b-rapeport/e7be33a0-830c-4bdb-9678-e7be665102d6
Source feed: FDA_Inspections

> FDA Inspection 805250 for Kevin B Rapeport on October 18, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 805250
- Company Name: Kevin B Rapeport
- Inspection Date: 2012-10-18
- 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/kevin-b-rapeport/02e88f16-d151-49a0-a214-8c84490bd7ab

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