# FDA Inspection 894795 - Geister Medizintecknik Gmbh - March 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/geister-medizintecknik-gmbh/4cc762b2-2cdd-4984-bc75-0f21214625d4
Source feed: FDA_Inspections

> FDA Inspection 894795 for Geister Medizintecknik Gmbh on March 27, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894795
- Company Name: Geister Medizintecknik Gmbh
- Inspection Date: 2014-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1019976 - 2016-10-26](https://www.keypedia.com/records/fda_inspections/geister-medizintecknik-gmbh/e40ca9fb-0c31-41db-b55f-3ec7dc7edfab)
- [FDA Inspection 894795 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/geister-medizintecknik-gmbh/d662ee53-3f07-42e6-a19b-25060a8a5959)

Company: https://www.keypedia.com/companies/geister-medizintecknik-gmbh/6b92f54b-5da1-4ae0-a42f-d9f7afd5265d

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