# FDA Inspection 576561 - Daewoo Electronics Corp. - March 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/daewoo-electronics-corp/917aca65-0dca-4b9b-b4c1-337a7530c959
Source feed: FDA_Inspections

> FDA Inspection 576561 for Daewoo Electronics Corp. on March 30, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 576561
- Company Name: Daewoo Electronics Corp.
- Inspection Date: 2009-03-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/daewoo-electronics-corp/10ef8f98-24a3-40b3-b801-c9d6b9965530

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