# Delta Med SpA – FDA Inspection, May 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/delta-med-spa/d701ca5d-a8a7-44f5-a2f9-206a85047023
Source feed: FDA_Inspections

> FDA inspection 780033 of Delta Med SpA, May 03, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 780033
- Company Name: Delta Med SpA
- Inspection Date: 2012-05-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1051764 - 2018-01-25](https://www.keypedia.com/records/fda_inspections/delta-med-spa/18194c00-ef75-446c-a0fe-e07cb58212b8)
- [FDA Inspection 1029762 - 2017-10-26](https://www.keypedia.com/records/fda_inspections/delta-med-spa/ecffd11a-5eb7-4261-8c2e-28c01ea534c5)

Company: https://www.keypedia.com/companies/delta-med-spa/0f883efb-8062-4c4d-b9bb-d4b4f468fe6d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7