# FDA Inspection 805290 - Synergy Health North America - November 15, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/synergy-health-north-america/fc94039d-560e-41cb-be79-162b8acc3bdc/
Source feed: FDA_Inspections

> FDA Inspection 805290 for Synergy Health North America on November 15, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805290
- Company Name: Synergy Health North America
- Inspection Date: 2012-11-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 998145 - 2016-10-17](https://www.globalkeysolutions.net/api/records/fda_inspections/synergy-health-north-america/186484c0-6004-4169-9c27-26a719bfe4fb/)
- [FDA Inspection 998145 - 2016-10-17](https://www.globalkeysolutions.net/api/records/fda_inspections/synergy-health-north-america/f43990e5-aa5f-48c2-bd54-0c0a254ad8b1/)

Company: https://www.globalkeysolutions.net/companies/synergy-health-north-america/3f88922a-2cf7-4bde-a845-82d847e06003

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