# Bieffe Medital SpA – FDA Inspection, Oct 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/bieffe-medital-spa/3944e3e4-a9ae-4efc-a936-e42684da688a
Source feed: FDA_Inspections

> FDA inspection 621498 of Bieffe Medital SpA, October 16, 2009. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 621498
- Company Name: Bieffe Medital SpA
- Inspection Date: 2009-10-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1235890 - 2023-11-17
- FDA Inspection 1128816 - 2019-06-28
- [FDA Inspection 1126215 - 2018-09-28](https://www.keypedia.com/records/fda_inspections/bieffe-medital-spa/99e7c618-e88d-42ea-aca7-ab4e0388b5ea)
- [FDA Inspection 1057424 - 2018-05-29](https://www.keypedia.com/records/fda_inspections/bieffe-medital-spa/15f9154b-0a35-437c-b061-47e77172dd41)
- FDA Inspection 945063 - 2015-09-22

Company: https://www.keypedia.com/companies/bieffe-medital-spa/a6b2f058-d687-4e04-bfd3-8b59ed1aeddd

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