# FDA Inspection 848893 - Interojo Inc. - July 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/interojo-inc/3d21d6c0-b2b2-47af-aadb-0b68158b5a6c
Source feed: FDA_Inspections

> FDA Inspection 848893 for Interojo Inc. on July 18, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848893
- Company Name: Interojo Inc.
- Inspection Date: 2013-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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