# BIOTEC ITALIA – FDA Inspection, Aug 8, 2024

Source: https://www.keypedia.com/records/fda_inspections/biotec-italia/04cc9729-4b46-4e72-9702-98b9f58e26c0
Source feed: FDA_Inspections

> FDA inspection 1249530 of BIOTEC ITALIA, August 08, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1249530
- Company Name: BIOTEC ITALIA
- Inspection Date: 2024-08-08
- 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: 2

## Related Officers

- Melissa A. Zuppe

Company: https://www.keypedia.com/companies/biotec-italia/88fdec83-d1c2-48ad-bf60-a1c9f6c6881b

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