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FDA Inspection
•Natus Manufacturing Limited•October 27, 2016

Natus Manufacturing Limited – FDA Inspection, Oct 27, 2016

Record Details

This FDA Inspection record concerns Natus Manufacturing Limited, with an inspection on October 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Natus Manufacturing Limited
Inspection Date
October 27, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Ashley A. Mutawakkil (Investigator)
View Company Profile

ID · ac081c4e-a572-40e3-85f6-ce78ee50ebbf

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
991399
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Natus Manufacturing Limited

2
DateClassificationOfficeProject area
August 30, 2019Not classifiedOffice of Inspections and Investigations
January 23, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Natus Manufacturing Limited
  • FDA Inspection 1122112 - 2019-08-30
  • FDA Inspection 863282 - 2014-01-23

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