FDA Inspection
Bruce G. Goldner, MDBruce G. Goldner, MD – FDA Inspection, Jan 22, 2016
Record Details
This FDA Inspection record concerns Bruce G. Goldner, MD, with an inspection on January 22, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bruce G. Goldner, MD
- Inspection Date
- January 22, 2016
- Product Type
- Devices
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ID · f0ce3544-149d-49b8-b49a-b7386d471552
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 955851
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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Other FDA inspections of Bruce G. Goldner, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 24, 2024 | Not classified | New York District Office |
Other documents for Bruce G. Goldner, MD
- FDA Inspection 1228370 - 2024-01-24
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