FDA Inspection
Robert L. Feldman, MDRobert L. Feldman, MD – FDA Inspection, Sep 24, 2010
Record Details
This FDA Inspection record concerns Robert L. Feldman, MD, with an inspection on September 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Robert L. Feldman, MD
- Inspection Date
- September 24, 2010
- Product Type
- Devices
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ID · b8e19afd-a362-47c5-bcff-504c87b6cbdb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 682936
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Robert L. Feldman, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2020 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 8, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Robert L. Feldman, MD
- FDA Inspection 1117567 - 2020-01-30
- FDA Inspection 772085 - 2012-03-08
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