# FDA Inspection 937481 - Herniamesh S.r.l - July 23, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/herniamesh-srl/57a9ad16-c4bc-4bea-a331-0afb201c431f
Source feed: FDA_Inspections

> FDA Inspection 937481 for Herniamesh S.r.l on July 23, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 937481
- Company Name: Herniamesh S.r.l
- Inspection Date: 2015-07-23
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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