# FDA Inspection 1019976 - Geister Medizintecknik Gmbh - October 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/geister-medizintecknik-gmbh/e40ca9fb-0c31-41db-b55f-3ec7dc7edfab
Source feed: FDA_Inspections

> FDA Inspection 1019976 for Geister Medizintecknik Gmbh on October 26, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019976
- Company Name: Geister Medizintecknik Gmbh
- Inspection Date: 2016-10-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 894795 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/geister-medizintecknik-gmbh/4cc762b2-2cdd-4984-bc75-0f21214625d4)
- [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