FDA Inspection
David J. Goldberg, MDDavid J. Goldberg, MD – FDA Inspection, Apr 27, 2012
Record Details
This FDA Inspection record concerns David J. Goldberg, MD, with an inspection on April 27, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- David J. Goldberg, MD
- Inspection Date
- April 27, 2012
- Product Type
- Devices
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ID · dae7f070-81ea-4acc-ac93-d56fa21588c1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 778732
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of David J. Goldberg, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 11, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 25, 2012 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for David J. Goldberg, MD
- FDA Inspection 1195696 - 2023-01-11
- FDA Inspection 804866 - 2012-10-25
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