# FDA Inspection 819217 - Manogg Medizintechnik OHG - January 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/manogg-medizintechnik-ohg/55da4dca-733c-4ae3-b141-b79fc7637cea
Source feed: FDA_Inspections

> FDA Inspection 819217 for Manogg Medizintechnik OHG on January 30, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819217
- Company Name: Manogg Medizintechnik OHG
- Inspection Date: 2013-01-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/manogg-medizintechnik-ohg/9c9bc49c-8b7f-45cf-bd59-8d0ef954d001

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