# FDA Inspection 850601 - Georg Alber GmbH & Co. KG - September 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/georg-alber-gmbh-co-kg/087942d8-ca85-4f28-9ff7-dd983bbbe855
Source feed: FDA_Inspections

> FDA Inspection 850601 for Georg Alber GmbH & Co. KG on September 19, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 850601
- Company Name: Georg Alber GmbH & Co. KG
- Inspection Date: 2013-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 850601 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/georg-alber-gmbh-co-kg/a0f39c61-f1db-4873-a16f-20ab7d9e05d5)

Company: https://www.keypedia.com/companies/georg-alber-gmbh-co-kg/19cd8845-5a69-4a05-bab0-bb6011843897

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