# FDA Inspection 917548 - Dream Systems, LLC - March 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/dream-systems-llc/bfb3e85b-c6f1-4c89-b4bf-44aca52aa12a
Source feed: FDA_Inspections

> FDA Inspection 917548 for Dream Systems, LLC on March 20, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 917548
- Company Name: Dream Systems, LLC
- Inspection Date: 2015-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 917548 - 2015-03-20](https://www.keypedia.com/records/fda_inspections/dream-systems-llc/821b58b9-1c5c-4c25-8496-7a54dde9b67c)
- [FDA Inspection 672186 - 2010-07-27](https://www.keypedia.com/records/fda_inspections/dream-systems-llc/beb25b4d-c179-4844-867c-fb7ac77ea040)
- [FDA Inspection 672186 - 2010-07-27](https://www.keypedia.com/records/fda_inspections/dream-systems-llc/1230f7c9-5362-4ab7-9363-20b2249f3b22)

Company: https://www.keypedia.com/companies/dream-systems-llc/02f74c9f-7751-46f5-aaac-83895092dd0a

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