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FDA Inspection
•Mediplast Israel Ltd.•August 31, 2017

Mediplast Israel Ltd. – FDA Inspection, Aug 31, 2017

Record Details

This FDA Inspection record concerns Mediplast Israel Ltd., with an inspection on August 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Mediplast Israel Ltd.
Inspection Date
August 31, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Lori S. Lawless (Company Rep)
  • Wanda B Coats (Issuing Officer)
View Company Profile

ID · 9ccea007-9663-4dfe-9a48-1d7034d42e8c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1035247
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Mediplast Israel Ltd.

3
DateClassificationOfficeProject area
April 3, 2014VAICenter for Devices and Radiological HealthBioresearch Monitoring
July 26, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
May 2, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Mediplast Israel Ltd.
  • FDA Inspection 877274 - 2014-04-03
  • FDA Inspection 740206 - 2011-07-26
  • FDA Inspection 663170 - 2010-05-02

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