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FDA Inspection
•SSCOR Inc•January 17, 2018

SSCOR Inc – FDA Inspection, Jan 17, 2018

Record Details

This FDA Inspection record concerns SSCOR Inc, with an inspection on January 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
SSCOR Inc
Inspection Date
January 17, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kelvin Cheung (Issuing Officer)
View Company Profile

ID · 49b9606b-b691-4f0c-8158-fa0dff84a406

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1038101
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.30(f)Design verification - documentation
  2. 21 CFR 820.90(a)Nonconforming product control

Full citation text and observation details available on the Dashboard.

Other FDA inspections of SSCOR Inc

3
DateClassificationOfficeProject area
October 14, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 13, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 18, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for SSCOR Inc
  • FDA Inspection 899381 - 2014-10-14
  • FDA Inspection 731375 - 2011-06-13
  • FDA Inspection 646641 - 2010-02-18

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