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FDA Inspection
•Hill-Rom Inc•November 10, 2017

Hill-Rom Inc – FDA Inspection, Nov 10, 2017

Record Details

This FDA Inspection record concerns Hill-Rom Inc, with an inspection on November 10, 2017, issued by the Detroit District Office, covering medical devices & rad health.

Company
Hill-Rom Inc
Inspection Date
November 10, 2017
Product Type
Medical Devices & Rad Health
Office
Detroit District Office
View Company Profile

ID · 4fa4e110-8043-408c-9970-7cee9041e91e

Inspection Facts

Inspection number
1051809
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Hill-Rom Inc

8
DateClassificationOfficeProject area
April 12, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 19, 2021VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 19, 2014VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 13, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
January 11, 2013OAICenter for Devices and Radiological HealthCompliance: Devices
View all 8 other inspections on the company page
Other documents for Hill-Rom Inc
  • FDA Inspection 1232908 - 2024-04-12
  • FDA Inspection 1157281 - 2021-11-19
  • FDA Inspection 911524 - 2014-12-19
  • FDA Inspection 865826 - 2014-02-13
  • FDA Inspection 807507 - 2013-01-11

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