FDA Inspection
Brent McLaurin, M.D.Brent McLaurin, M.D. – FDA Inspection, Jun 9, 2009
Record Details
This FDA Inspection record concerns Brent McLaurin, M.D., with an inspection on June 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Brent McLaurin, M.D.
- Inspection Date
- June 9, 2009
- Product Type
- Devices
View Company Profile
ID · c5e0924b-d740-4fc0-8ab8-29b1766f3a17
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 607322
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
4- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Brent McLaurin, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 8, 2020 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Brent McLaurin, M.D.
- FDA Inspection 1116393 - 2020-01-08
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