FDA Inspection
Heartland Regional Med Center IRBHeartland Regional Med Center IRB – FDA Inspection, Nov 7, 2013
Record Details
This FDA Inspection record concerns Heartland Regional Med Center IRB, with an inspection on November 7, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 7, 2013
- Product Type
- Devices
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ID · 92868f5a-06de-4384-bce3-ed5cb4fc1cce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 854225
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 56.115(a)(2)Minutes of IRB meetings
- 21 CFR 56.107(e)Conflict of interest
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Other FDA inspections of Heartland Regional Med Center IRB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2025 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Heartland Regional Med Center IRB
- FDA Inspection 1276341 - 2025-07-21
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