# FDA Inspection 938632 - Hyperion Medical Technologies Inc - July 09, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/hyperion-medical-technologies-inc/67dbf017-27ea-44b5-a526-d2cfd58f0c65
Source feed: FDA_Inspections

> FDA Inspection 938632 for Hyperion Medical Technologies Inc on July 09, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938632
- Company Name: Hyperion Medical Technologies Inc
- Inspection Date: 2015-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1030690 - 2017-06-20](https://www.globalkeysolutions.net/records/fda_inspections/hyperion-medical-technologies-inc/be165b5d-3a2f-4156-951f-915e882b9d22)
- [FDA Inspection 938632 - 2015-07-09](https://www.globalkeysolutions.net/records/fda_inspections/hyperion-medical-technologies-inc/dcb6f932-e8ac-4820-af5d-b772897e292e)

Company: https://www.globalkeysolutions.net/companies/hyperion-medical-technologies-inc/964d1e1d-9156-45e5-9428-da750f90546a

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