FDA Inspection
Vincent DiGiovanni, DOVincent DiGiovanni, DO – FDA Inspection, Aug 18, 2025
Record Details
This FDA Inspection record concerns Vincent DiGiovanni, DO, with an inspection on August 18, 2025, issued by the Philadelphia District Office, covering medical devices & rad health.
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ID · 50d77eb3-3a96-445a-836e-a9c3895bcedf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1278904
- FDA center
- Medical Devices & Rad Health
- Project area
- Product Evaluation: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(3)Investigator's subject records inadequate
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