FDA Inspection
Mercy Research IRBMercy Research IRB – FDA Inspection, Jan 23, 2009
Record Details
This FDA Inspection record concerns Mercy Research IRB, with an inspection on January 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Mercy Research IRB
- Inspection Date
- January 23, 2009
- Product Type
- Devices
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ID · 83abe8cd-c1f4-4420-98aa-b8ebdad76c51
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 559346
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 56.115(a)(5)List of members
- 21 CFR 56.108(a)(1)Initial and continuing reviews
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Mercy Research IRB
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2022 | NAI | Bioresearch Monitoring | |
| February 16, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| June 15, 2015 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Mercy Research IRB
- FDA Inspection 1170288 - 2022-04-11
- FDA Inspection 1045009 - 2018-02-16
- FDA Inspection 930451 - 2015-06-15
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