# FDA Inspection 1005634 - GELITA DEUTSCHLAND GMBH - February 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/gelita-deutschland-gmbh/b6df50e6-497f-4ac5-a4c3-b364dc93910e
Source feed: FDA_Inspections

> FDA Inspection 1005634 for GELITA DEUTSCHLAND GMBH on February 10, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005634
- Company Name: GELITA DEUTSCHLAND GMBH
- Inspection Date: 2017-02-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/gelita-deutschland-gmbh/d04659fa-805e-40b9-9498-18978e6f384c

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