# FDA Inspection 756823 - ACTIVAERO GMBH - November 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/activaero-gmbh/4c952c75-4a2b-47f4-9cd3-1b8cf30b091c
Source feed: FDA_Inspections

> FDA Inspection 756823 for ACTIVAERO GMBH on November 24, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 756823
- Company Name: ACTIVAERO GMBH
- Inspection Date: 2011-11-24
- 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/activaero-gmbh/12a3e936-dbc0-457b-80f8-da0683dc71e4

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