FDA Inspection
Robert A. Weiss, M.D.Robert A. Weiss, M.D. – FDA Inspection, Oct 29, 2019
Record Details
This FDA Inspection record concerns Robert A. Weiss, M.D., with an inspection on October 29, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Robert A. Weiss, M.D.
- Inspection Date
- October 29, 2019
- Product Type
- Devices
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ID · 35b047f3-4f90-49a0-842f-0dd346436397
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1107837
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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Other FDA inspections of Robert A. Weiss, M.D.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 19, 2023 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| October 27, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 26, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Robert A. Weiss, M.D.
- FDA Inspection 1206481 - 2023-05-19
- FDA Inspection 947315 - 2015-10-27
- FDA Inspection 846083 - 2013-08-26
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