# FDA Inspection 1038015 - Venni Instruments Inc - January 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/venni-instruments-inc/fe680c97-4eec-4692-909e-0321507460e9/
Source feed: FDA_Inspections

> FDA Inspection 1038015 for Venni Instruments Inc on January 17, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038015
- Company Name: Venni Instruments Inc
- Inspection Date: 2018-01-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1038015 - 2018-01-17](https://www.globalkeysolutions.net/api/records/fda_inspections/venni-instruments-inc/1818e33c-de72-4bec-970e-d981913e9090/)
- [FDA Inspection 920978 - 2015-03-31](https://www.globalkeysolutions.net/api/records/fda_inspections/venni-instruments-inc/10e18c79-3999-476e-8eb4-55623cb641f0/)
- [FDA Inspection 920978 - 2015-03-31](https://www.globalkeysolutions.net/api/records/fda_inspections/venni-instruments-inc/8515e4f5-89ea-47fa-898b-17b505c41852/)
- [FDA Inspection 810371 - 2012-12-13](https://www.globalkeysolutions.net/api/records/fda_inspections/venni-instruments-inc/86760eca-09aa-4b8c-ab90-16ef3195c9be/)

Company: https://www.globalkeysolutions.net/companies/venni-instruments-inc/ec6009bf-be86-4e20-afc2-e37d95191d1e

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