# FDA Inspection 1038529 - HTL-Strefa Sp.Zoo - December 14, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/htl-strefa-spzoo/fdcfdf22-fdaf-4b07-a521-5805474f69b7/
Source feed: FDA_Inspections

> FDA Inspection 1038529 for HTL-Strefa Sp.Zoo on December 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038529
- Company Name: HTL-Strefa Sp.Zoo
- Inspection Date: 2017-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1038529 - 2017-12-14](https://www.globalkeysolutions.net/api/records/fda_inspections/htl-strefa-spzoo/6d5b70e4-c27e-44d1-b294-20543d9df99b/)

Company: https://www.globalkeysolutions.net/companies/htl-strefa-spzoo/41962032-242e-4725-89f8-081b814cd375

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