# FDA Inspection 830026 - Biolitec, Inc. - April 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/biolitec-inc/119d319f-2e1b-4b35-b7c6-57398a54ccde
Source feed: FDA_Inspections

> FDA Inspection 830026 for Biolitec, Inc. on April 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830026
- Company Name: Biolitec, Inc.
- Inspection Date: 2013-04-26
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 830026 - 2013-04-26](https://www.keypedia.com/records/fda_inspections/biolitec-inc/87e08a10-0eec-427c-9909-b9913c8e7095)
- [FDA Inspection 648180 - 2010-02-23](https://www.keypedia.com/records/fda_inspections/biolitec-inc/2dc01484-057d-440c-9d5f-c8c3607dab5b)
- [FDA Inspection 648180 - 2010-02-23](https://www.keypedia.com/records/fda_inspections/biolitec-inc/791206ea-9d63-4df2-8753-f24a6c948b2d)
- [FDA Inspection 648180 - 2010-02-23](https://www.keypedia.com/records/fda_inspections/biolitec-inc/590cad7b-1080-41d2-b70d-169d6231c3ae)

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