# HTL-Strefa, Inc. – FDA Inspection, Feb 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/htl-strefa-inc/bd3c046b-9521-41de-ad05-8305aabf407d
Source feed: FDA_Inspections

> FDA inspection 821688 of HTL-Strefa, Inc., February 21, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 966079 - 2016-02-11](https://www.keypedia.com/records/fda_inspections/htl-strefa-inc/287d64f7-0de4-4158-b52a-75f80c4285b7)

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

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