FDA Inspection
Hill-Rom Manufacturing, Inc.Hill-Rom Manufacturing, Inc. – FDA Inspection, Apr 15, 2009
Record Details
This FDA Inspection record concerns Hill-Rom Manufacturing, Inc., with an inspection on April 15, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hill-Rom Manufacturing, Inc.
- Inspection Date
- April 15, 2009
- Product Type
- Devices
View Company Profile
ID · 8761519e-f5c7-4a68-9973-c029dbff8b4f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 575745
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Hill-Rom Manufacturing, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 10, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 15, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Hill-Rom Manufacturing, Inc.
- FDA Inspection 857032 - 2013-11-21
- FDA Inspection 769788 - 2012-02-10
- FDA Inspection 576910 - 2009-04-15
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