# Interojo Inc. – FDA Inspection, Jul 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/interojo-inc/66be8e4b-ccdf-4f72-abb7-61f227e7f274
Source feed: FDA_Inspections

> FDA inspection 848893 of Interojo Inc., July 18, 2013. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 848893
- Company Name: Interojo Inc.
- Inspection Date: 2013-07-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1101815 - 2019-08-29](https://www.keypedia.com/records/fda_inspections/interojo-inc/fe72b567-386b-4e3e-847a-491f4a30a1f0)
- [FDA Inspection 1124008 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/interojo-inc/cc2350d5-42e1-4eb1-b978-9da469022639)

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