# FDA Inspection 642925 - Scholten Surgical Instruments - January 21, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/scholten-surgical-instruments/e1b04825-3e5b-42ef-a434-9da9213cbef2
Source feed: FDA_Inspections

> FDA Inspection 642925 for Scholten Surgical Instruments on January 21, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 642925
- Company Name: Scholten Surgical Instruments
- Inspection Date: 2010-01-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 904917 - 2014-12-05](https://www.globalkeysolutions.net/records/fda_inspections/scholten-surgical-instruments/f0177e10-fc78-4cc5-9452-08e91c162231)
- [FDA Inspection 904917 - 2014-12-05](https://www.globalkeysolutions.net/records/fda_inspections/scholten-surgical-instruments/fdb88bfc-cb99-4579-ac29-c3449cb9a8d5)

Company: https://www.globalkeysolutions.net/companies/scholten-surgical-instruments/8fcd04f7-b69c-4a6c-aa5a-75cd7487f369

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