# FDA Inspection 1101815 - Interojo Inc. - August 29, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/interojo-inc/fe72b567-386b-4e3e-847a-491f4a30a1f0/
Source feed: FDA_Inspections

> FDA Inspection 1101815 for Interojo Inc. on August 29, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101815
- Company Name: Interojo Inc.
- Inspection Date: 2019-08-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101815 - 2019-08-29](https://www.globalkeysolutions.net/api/records/fda_inspections/interojo-inc/80736847-3d7f-4ea6-b3d4-d00754125a99/)
- [FDA Inspection 848893 - 2013-07-18](https://www.globalkeysolutions.net/api/records/fda_inspections/interojo-inc/3d21d6c0-b2b2-47af-aadb-0b68158b5a6c/)
- [FDA Inspection 848893 - 2013-07-18](https://www.globalkeysolutions.net/api/records/fda_inspections/interojo-inc/66be8e4b-ccdf-4f72-abb7-61f227e7f274/)

Company: https://www.globalkeysolutions.net/companies/interojo-inc/afd7a693-fcdd-4cc6-81cc-423cfcc2e392

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