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FDA Inspection
•Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies•April 19, 2016

Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies – FDA Inspection, Apr 19, 2016

Record Details

This FDA Inspection record concerns Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies, with an inspection on April 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies
Inspection Date
April 19, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fd2b12e5-bce5-4f0e-92f8-47284db41b2b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
968352
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies

9
DateClassificationOfficeProject area
August 1, 2025Not classifiedNew England District Office
March 9, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 12, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 21, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 9, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
View all 9 other inspections on the company page
Other documents for Isomedix Operations, Inc. dba Steris Applied Sterilization Technologies
  • FDA Inspection 1273685 - 2025-08-01
  • FDA Inspection 1122029 - 2020-03-09
  • FDA Inspection 1076536 - 2018-12-12
  • FDA Inspection 915631 - 2015-01-21
  • FDA Inspection 874257 - 2014-04-09

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