# FDA Inspection 821688 - HTL-Strefa, Inc. - February 21, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/htl-strefa-inc/a07e7b3c-b29b-4505-a29f-6d29a6701261
Source feed: FDA_Inspections

> FDA Inspection 821688 for HTL-Strefa, Inc. on February 21, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821688
- Company Name: HTL-Strefa, Inc.
- Inspection Date: 2013-02-21
- 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 966079 - 2016-02-11](https://www.globalkeysolutions.net/records/fda_inspections/htl-strefa-inc/287d64f7-0de4-4158-b52a-75f80c4285b7)
- [FDA Inspection 821688 - 2013-02-21](https://www.globalkeysolutions.net/records/fda_inspections/htl-strefa-inc/bd3c046b-9521-41de-ad05-8305aabf407d)

Company: https://www.globalkeysolutions.net/companies/htl-strefa-inc/01f3c516-4993-40fb-8704-65f4a69ef4df

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