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FDA Inspection
•DePuy Spine, Inc.•February 10, 2012

DePuy Spine, Inc. – FDA Inspection, Feb 10, 2012

Record Details

This FDA Inspection record concerns DePuy Spine, Inc., with an inspection on February 10, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
DePuy Spine, Inc.
Inspection Date
February 10, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · d542b6b9-5e8f-45f8-ba7b-a016e1ac47ee

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
767079
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

2
  1. 21 CFR 812.46(a)Sponsor securing investigator compliance
  2. 21 CFR 812.40Sponsors" general responsibilities

Full citation text and observation details available on the Dashboard.

Other FDA inspections of DePuy Spine, Inc.

6
DateClassificationOfficeProject area
April 18, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 16, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
June 11, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
April 28, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
April 21, 2009NAICenter for Devices and Radiological HealthBioresearch Monitoring
View all 6 other inspections on the company page
Other documents for DePuy Spine, Inc.
  • FDA Inspection 1090256 - 2019-04-18
  • FDA Inspection 1021012 - 2017-06-16
  • FDA Inspection 787390 - 2012-06-11
  • FDA Inspection 580522 - 2009-04-28
  • FDA Inspection 577762 - 2009-04-21

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