# FDA Inspection 639022 - Spectrum Designs Inc - January 20, 2010

Source: https://www.keypedia.com/records/fda_inspections/spectrum-designs-inc/731e11fc-1bb1-4507-911e-ba919406d03c
Source feed: FDA_Inspections

> FDA Inspection 639022 for Spectrum Designs Inc on January 20, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 639022
- Company Name: Spectrum Designs Inc
- Inspection Date: 2010-01-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 914394 - 2015-02-18](https://www.keypedia.com/records/fda_inspections/spectrum-designs-inc/a40de87f-3f53-4377-a24a-f49876a687a9)
- [FDA Inspection 639022 - 2010-01-20](https://www.keypedia.com/records/fda_inspections/spectrum-designs-inc/b0aeaea5-ef0c-4900-8ae3-f9bea224670b)

Company: https://www.keypedia.com/companies/spectrum-designs-inc/642b4ce5-a8aa-4c74-9a58-927e3a7024fa

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