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

Source: https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/57475087-ee67-4fef-885b-7208a4551bf9
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: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1254940 - 2024-11-21](https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/0b33dd8f-1a70-4c08-8b93-75e5f9c0d6ae)
- [FDA Inspection 1254940 - 2024-11-21](https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/f8420bab-0187-4b06-bb1e-40aee1b4936e)
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- [FDA Inspection 981516 - 2016-07-01](https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/6a445b55-8eb1-48a6-8291-b1eba22f4e43)
- [FDA Inspection 981516 - 2016-07-01](https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/ebcf1e6a-b51a-4496-8124-9dd406c96053)

Company: https://www.globalkeysolutions.net/companies/herniamesh-srl/e76206de-b76c-4fe8-87ed-a7369b90a112

Office: https://www.globalkeysolutions.net/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8