# FDA Inspection 649466 - Lakeshore Technologies Inc - February 22, 2010

Source: https://www.keypedia.com/records/fda_inspections/lakeshore-technologies-inc/7911830d-abb5-4799-a20d-3af49612759a
Source feed: FDA_Inspections

> FDA Inspection 649466 for Lakeshore Technologies Inc on February 22, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 649466
- Company Name: Lakeshore Technologies Inc
- Inspection Date: 2010-02-22
- 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 649466 - 2010-02-22](https://www.keypedia.com/records/fda_inspections/lakeshore-technologies-inc/eb6c7548-fac4-478c-91a0-93d9d97a061e)

Company: https://www.keypedia.com/companies/lakeshore-technologies-inc/8247a09d-2fec-428f-ad9e-c1496bebc0c4

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