# FDA Inspection 859270 - Guidemia Technologies Inc. - December 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/guidemia-technologies-inc/ff06699e-4f86-435c-8205-b3bdbee07fb2/
Source feed: FDA_Inspections

> FDA Inspection 859270 for Guidemia Technologies Inc. on December 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 859270
- Company Name: Guidemia Technologies Inc.
- Inspection Date: 2013-12-12
- 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 1081235 - 2019-02-11](https://www.globalkeysolutions.net/api/records/fda_inspections/guidemia-technologies-inc/15837754-2496-4f59-9fb2-b1ac07784071/)
- [FDA Inspection 859270 - 2013-12-12](https://www.globalkeysolutions.net/api/records/fda_inspections/guidemia-technologies-inc/f1a5b43d-b2a5-4a0a-8818-a520b096655a/)

Company: https://www.globalkeysolutions.net/companies/guidemia-technologies-inc/a4f32aed-30e9-49cb-a1e2-6efe08778b58

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