FDA Inspection
Paul Arnold, MDPaul Arnold, MD – FDA Inspection, Sep 23, 2021
Record Details
This FDA Inspection record concerns Paul Arnold, MD, with an inspection on September 23, 2021, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Paul Arnold, MD
- Inspection Date
- September 23, 2021
- Product Type
- Devices
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ID · c2aadeb6-cf89-47f5-a003-4c9bd2e9c7bb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1152474
- 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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