# FDA Inspection 665318 - Solafeet, Inc. - May 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/solafeet-inc/38a3d1d6-9a04-4465-a0ec-61d40c843a97
Source feed: FDA_Inspections

> FDA Inspection 665318 for Solafeet, Inc. on May 28, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 665318
- Company Name: Solafeet, Inc.
- Inspection Date: 2010-05-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 665318 - 2010-05-28](https://www.keypedia.com/records/fda_inspections/solafeet-inc/76f11cce-5216-460e-8477-4289f8f05516)
- [FDA Inspection 665318 - 2010-05-28](https://www.keypedia.com/records/fda_inspections/solafeet-inc/e54a8f57-a4b0-430a-922a-25f61770d485)

Company: https://www.keypedia.com/companies/solafeet-inc/b7f6f5f0-98cc-4047-8469-758a31ba9a05

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