FDA Inspection
Hill-Rom IncHill-Rom Inc – FDA Inspection, Jan 23, 2009
Record Details
This FDA Inspection record concerns Hill-Rom Inc, with an inspection on January 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hill-Rom Inc
- Inspection Date
- January 23, 2009
- Product Type
- Devices
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ID · cc7288c0-d5e9-45cf-b042-3d28fb6d2c78
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 556638
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.100(a)(3)Identifying corrective & preventive actions
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Other FDA inspections of Hill-Rom Inc
8| Date | Classification | Office | Project area |
|---|---|---|---|
| April 12, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 19, 2021 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 10, 2017 | Not classified | Detroit District Office | |
| December 19, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 13, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hill-Rom Inc
- FDA Inspection 1232908 - 2024-04-12
- FDA Inspection 1157281 - 2021-11-19
- FDA Inspection 1051809 - 2017-11-10
- FDA Inspection 911524 - 2014-12-19
- FDA Inspection 865826 - 2014-02-13
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