FDA Inspection
Marianne Brodmann, MDMarianne Brodmann, MD – FDA Inspection, Mar 22, 2019
Record Details
This FDA Inspection record concerns Marianne Brodmann, MD, with an inspection on March 22, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Lequita M. Mayhew (Issuing Officer)
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ID · b13b9af1-1be6-4dec-a360-f5b83c9e5cc2
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1083796
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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