# FDA Inspection 669646 - Harps Europe Manufacturing - May 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/harps-europe-manufacturing/870b4446-e23f-4d91-860d-a68f269e79b4
Source feed: FDA_Inspections

> FDA Inspection 669646 for Harps Europe Manufacturing on May 28, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 669646
- Company Name: Harps Europe Manufacturing
- Inspection Date: 2010-05-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 669646 - 2010-05-28](https://www.keypedia.com/records/fda_inspections/harps-europe-manufacturing/32b26f2c-891f-4891-8bfb-9481a0a86918)

Company: https://www.keypedia.com/companies/harps-europe-manufacturing/2d8bb4fa-44b6-449d-89d8-09a187a1a8ec

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