# Interojo Inc. – FDA Inspection, Aug 29, 2019

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

> FDA inspection 1101815 of Interojo Inc., August 29, 2019. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1124008 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/interojo-inc/cc2350d5-42e1-4eb1-b978-9da469022639)
- [FDA Inspection 848893 - 2013-07-18](https://www.keypedia.com/records/fda_inspections/interojo-inc/66be8e4b-ccdf-4f72-abb7-61f227e7f274)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

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