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FDA Inspection
•I.E.M. Gmbh•October 21, 2011

I.E.M. Gmbh – FDA Inspection, Oct 21, 2011

Record Details

This FDA Inspection record concerns I.E.M. Gmbh, with an inspection on October 21, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
I.E.M. Gmbh
Inspection Date
October 21, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 83009436-6669-4709-bce1-48bbd14e00a7

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
753156
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of I.E.M. Gmbh

2
DateClassificationOfficeProject area
January 24, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
February 19, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for I.E.M. Gmbh
  • FDA Inspection 818868 - 2013-01-24
  • FDA Inspection 571413 - 2009-02-19

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