# FDA Inspection 1063743 - Amann Girrbach North America, L.P. - August 29, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/amann-girrbach-north-america-lp/fc66fff3-4929-451e-908c-1d1f4d944e71/
Source feed: FDA_Inspections

> FDA Inspection 1063743 for Amann Girrbach North America, L.P. on August 29, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063743
- Company Name: Amann Girrbach North America, L.P.
- Inspection Date: 2018-08-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1063743 - 2018-08-29](https://www.globalkeysolutions.net/api/records/fda_inspections/amann-girrbach-north-america-lp/0976a759-9e3a-4072-90f0-1779c3029f05/)

Company: https://www.globalkeysolutions.net/companies/amann-girrbach-north-america-lp/84867189-9d0a-498e-ab59-618c43265eca

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