FDA Inspection
Grossbard Lee, MDGrossbard Lee, MD – FDA Inspection, Aug 21, 2014
Record Details
This FDA Inspection record concerns Grossbard Lee, MD, with an inspection on August 21, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Grossbard Lee, MD
- Inspection Date
- August 21, 2014
- Product Type
- Devices
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ID · 24559359-a2e9-413e-8c2b-dd529113b9e4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 892529
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of informed consent
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