# FDA Inspection 1089571 - Inventus Power, Inc. - April 12, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/inventus-power-inc/193399e7-4f1d-4dc2-8917-be4c495970b2
Source feed: FDA_Inspections

> FDA Inspection 1089571 for Inventus Power, Inc. on April 12, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089571
- Company Name: Inventus Power, Inc.
- Inspection Date: 2019-04-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1089571 - 2019-04-12](https://www.globalkeysolutions.net/records/fda_inspections/inventus-power-inc/0c1f43b7-9444-46dc-8c8d-19af5ea5d6b9)

Company: https://www.globalkeysolutions.net/companies/inventus-power-inc/97b83e13-5e6a-4d78-9acc-8a7a6a553601

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