# FDA Inspection 893050 - Peter Whang, MD - August 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/peter-whang-md/d260cd03-d12f-426e-9290-c176a89060a0
Source feed: FDA_Inspections

> FDA Inspection 893050 for Peter Whang, MD on August 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893050
- Company Name: Peter Whang, MD
- Inspection Date: 2014-08-07
- 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/peter-whang-md/821422fa-577d-447a-b35b-f5d81204a28e

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