# FDA Inspection 553121 - Solon Manufacturing Company - December 02, 2008

Source: https://www.globalkeysolutions.net/records/fda_inspections/solon-manufacturing-company/fb9049c3-3bf7-4fe8-b0a2-4a412ebf6093/
Source feed: FDA_Inspections

> FDA Inspection 553121 for Solon Manufacturing Company on December 02, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 553121
- Company Name: Solon Manufacturing Company
- Inspection Date: 2008-12-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 553121 - 2008-12-02](https://www.globalkeysolutions.net/api/records/fda_inspections/solon-manufacturing-company/35edfb5e-2ab7-4476-9ac0-ec6b904a82c3/)

Company: https://www.globalkeysolutions.net/companies/solon-manufacturing-company/0d973c41-b736-41f6-b1e6-7d050fb227a6

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