# FDA Inspection 802887 - Klockner Of North America - October 03, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/klockner-of-north-america/3aba4384-e2a2-46cf-8dbc-44a76c4aaa14
Source feed: FDA_Inspections

> FDA Inspection 802887 for Klockner Of North America on October 03, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802887
- Company Name: Klockner Of North America
- Inspection Date: 2012-10-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/klockner-of-north-america/feb199c7-0277-4e6d-83c3-dca7bcde5a8a

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