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FDA Inspection
•Collimare, LLC•August 14, 2019

Collimare, LLC – FDA Inspection, Aug 14, 2019

Record Details

This FDA Inspection record concerns Collimare, LLC, with an inspection on August 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Collimare, LLC
Inspection Date
August 14, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Christine I. Shaw (Company Rep)
View Company Profile

ID · 8b7e62d2-bdac-4cc8-b9f3-cc9c9b0f951e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1100886
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Collimare, LLC

2
DateClassificationOfficeProject area
September 30, 2011NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
December 9, 2008NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Collimare, LLC
  • FDA Inspection 750110 - 2011-09-30
  • FDA Inspection 555085 - 2008-12-09

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