# FDA Inspection 820220 - Loewenstein Medical Technology GMBH + CO. KG - January 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/loewenstein-medical-technology-gmbh-co-kg/26811bef-e6ea-4114-b873-890870ef5bc7
Source feed: FDA_Inspections

> FDA Inspection 820220 for Loewenstein Medical Technology GMBH + CO. KG on January 31, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820220
- Company Name: Loewenstein Medical Technology GMBH + CO. KG
- Inspection Date: 2013-01-31
- 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/loewenstein-medical-technology-gmbh-co-kg/b20b870b-2877-4236-9fc4-613a4ad41590

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