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FDA Inspection
•Interojo Inc.•September 7, 2018

Interojo Inc. – FDA Inspection, Sep 7, 2018

Record Details

This FDA Inspection record concerns Interojo Inc., with an inspection on September 7, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Interojo Inc.
Inspection Date
September 7, 2018
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
View Company Profile

ID · cc2350d5-42e1-4eb1-b978-9da469022639

Inspection Facts

Inspection number
1124008
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Interojo Inc.

2
DateClassificationOfficeProject area
August 29, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
July 18, 2013VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Interojo Inc.
  • FDA Inspection 1101815 - 2019-08-29
  • FDA Inspection 848893 - 2013-07-18

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