# FDA Inspection 784218 - Kevin Waltz, OD, MD - May 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/kevin-waltz-od-md/1624193a-51ea-4829-952e-f390a16f4eab
Source feed: FDA_Inspections

> FDA Inspection 784218 for Kevin Waltz, OD, MD on May 23, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 784218
- Company Name: Kevin Waltz, OD, MD
- Inspection Date: 2012-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/kevin-waltz-od-md/fe9f027e-42e4-4150-a794-2fb124d47c09

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