FDA Inspection
Interojo Inc.Interojo Inc. – FDA Inspection, Jul 18, 2013
Record Details
This FDA Inspection record concerns Interojo Inc., with an inspection on July 18, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Interojo Inc.
- Inspection Date
- July 18, 2013
- Product Type
- Devices
View Company Profile
ID · 66be8e4b-ccdf-4f72-abb7-61f227e7f274
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 848893
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Interojo Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 29, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 7, 2018 | Not classified | Office of Inspections and Investigations |
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