# FDA Inspection 1249530 - BIOTEC ITALIA - August 08, 2024

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

> FDA Inspection 1249530 for BIOTEC ITALIA on August 08, 2024. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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