# FDA Inspection 1111640 - Amo Groningen BV - November 13, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/amo-groningen-bv/fabbbf0e-836f-4493-b131-c84f57a69756/
Source feed: FDA_Inspections

> FDA Inspection 1111640 for Amo Groningen BV on November 13, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1111640
- Company Name: Amo Groningen BV
- Inspection Date: 2019-11-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 870154 - 2014-02-13](https://www.globalkeysolutions.net/api/records/fda_inspections/amo-groningen-bv/2353bdce-685c-4d91-ba58-098e2d762cc1/)
- [FDA Inspection 663960 - 2010-04-22](https://www.globalkeysolutions.net/api/records/fda_inspections/amo-groningen-bv/962611e0-9d03-4189-9775-a4c113153f69/)
- [FDA Inspection 663960 - 2010-04-22](https://www.globalkeysolutions.net/api/records/fda_inspections/amo-groningen-bv/cc1ceb37-f2ca-44c6-bd1b-4298a390cea1/)

Company: https://www.globalkeysolutions.net/companies/amo-groningen-bv/fafe2bc5-482e-48c6-b339-35bb0ca0ee30

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