FDA Inspection
Leslie D. Grosinger, MDLeslie D. Grosinger, MD – FDA Inspection, Nov 25, 2013
Record Details
This FDA Inspection record concerns Leslie D. Grosinger, MD, with an inspection on November 25, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Leslie D. Grosinger, MD
- Inspection Date
- November 25, 2013
- Product Type
- Devices
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ID · d5807be3-e2d7-4e50-9116-1f52ddb120f1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 861292
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
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