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FDA Inspection
•Sendx Medical Inc•October 31, 2017

Sendx Medical Inc – FDA Inspection, Oct 31, 2017

Record Details

This FDA Inspection record concerns Sendx Medical Inc, with an inspection on October 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Sendx Medical Inc
Inspection Date
October 31, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Scott K. Zika (Issuing Officer)
View Company Profile

ID · 596b746d-d964-478d-bf3c-0a7290ad9c76

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1031157
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Sendx Medical Inc

4
DateClassificationOfficeProject area
December 4, 2025NAICenter for Devices and Radiological HealthCompliance: Devices
June 29, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
September 29, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 20, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Sendx Medical Inc
  • FDA Inspection 1295680 - 2025-12-04
  • FDA Inspection 1174815 - 2022-06-29
  • FDA Inspection 898205 - 2014-09-29
  • FDA Inspection 557428 - 2009-01-20

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