# FDA Inspection 648180 - Biolitec, Inc. - February 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/biolitec-inc/2dc01484-057d-440c-9d5f-c8c3607dab5b
Source feed: FDA_Inspections

> FDA Inspection 648180 for Biolitec, Inc. on February 23, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 648180
- Company Name: Biolitec, Inc.
- Inspection Date: 2010-02-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/biolitec-inc/4a2553ca-09ce-4f79-9ffa-63cc8559a1c6

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