# FDA Inspection 682329 - Liko North America, Subsidiary Of Hill-rom, Inc. - September 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/liko-north-america-subsidiary-of-hill-rom-inc/6a13da05-5c9a-4d2f-8e7b-3b55bb37dace
Source feed: FDA_Inspections

> FDA Inspection 682329 for Liko North America, Subsidiary Of Hill-rom, Inc. on September 24, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 682329
- Company Name: Liko North America, Subsidiary Of Hill-rom, Inc.
- Inspection Date: 2010-09-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 682329 - 2010-09-24](https://www.keypedia.com/records/fda_inspections/liko-north-america-subsidiary-of-hill-rom-inc/69890bdf-a397-42a6-983c-25bdc8c803a7)

Company: https://www.keypedia.com/companies/liko-north-america-subsidiary-of-hill-rom-inc/c0507e9c-f6f8-4714-807c-9ccbbff1db68

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