# Vincent DiGiovanni, DO – FDA Inspection, Aug 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/vincent-digiovanni-do/50d77eb3-3a96-445a-836e-a9c3895bcedf
Source feed: FDA_Inspections

> FDA inspection 1278904 of Vincent DiGiovanni, DO, August 18, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1278904
- Company Name: Vincent DiGiovanni, DO
- Inspection Date: 2025-08-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Philadelphia District Office
- Citation Count: 3

## Related Officers

- [Company Rep](https://www.keypedia.com/people/gabrielle-j-swain/55f33430-41dc-4fae-bac0-ec6ea340feb6)

Company: https://www.keypedia.com/companies/vincent-digiovanni-do/e1d07d35-5253-4c1e-835b-d15962c0349f

Office: https://www.keypedia.com/offices/philadelphia-district-office/c5ec7398-b3d5-4125-9793-fb7b972578d8