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FDA Inspection
•Intersurgical Inc•November 18, 2016

Intersurgical Inc – FDA Inspection, Nov 18, 2016

Record Details

This FDA Inspection record concerns Intersurgical Inc, with an inspection on November 18, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Intersurgical Inc
Inspection Date
November 18, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Nicholas C Mendiola (Issuing Officer)
View Company Profile

ID · 9e4bc443-22e4-4a6d-9efb-94b380bcbaad

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
993336
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Intersurgical Inc

4
DateClassificationOfficeProject area
September 11, 2024Not classifiedNew York District Office
November 1, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 29, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 21, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Intersurgical Inc
  • FDA Inspection 1249149 - 2024-09-11
  • FDA Inspection 1071317 - 2018-11-01
  • FDA Inspection 903122 - 2014-10-29
  • FDA Inspection 760050 - 2011-12-21

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