# FDA Inspection 1254940 - Herniamesh S.r.l - November 21, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/f8420bab-0187-4b06-bb1e-40aee1b4936e/
Source feed: FDA_Inspections

> FDA Inspection 1254940 for Herniamesh S.r.l on November 21, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1254940
- Company Name: Herniamesh S.r.l
- Inspection Date: 2024-11-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1254940 - 2024-11-21](https://www.globalkeysolutions.net/api/records/fda_inspections/herniamesh-srl/57475087-ee67-4fef-885b-7208a4551bf9/)
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Company: https://www.globalkeysolutions.net/companies/herniamesh-srl/e76206de-b76c-4fe8-87ed-a7369b90a112

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