# FDA Inspection 1070919 - Prollenium Medical Technologies Inc. - November 01, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/prollenium-medical-technologies-inc/935ea83c-fb57-4192-be65-12eb3ef41d41/
Source feed: FDA_Inspections

> FDA Inspection 1070919 for Prollenium Medical Technologies Inc. on November 01, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070919
- Company Name: Prollenium Medical Technologies Inc.
- Inspection Date: 2018-11-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1011040 - 2017-04-20](https://www.globalkeysolutions.net/api/records/fda_inspections/prollenium-medical-technologies-inc/d8e093dd-42be-47b9-a09d-6500aaa9a495/)

Company: https://www.globalkeysolutions.net/companies/prollenium-medical-technologies-inc/41fb7718-0d01-4d45-a62f-fb8e09c831e2

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