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

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

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Record Summary

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

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Record Information

Company

HTL-Strefa Sp.Zoo

Inspection Date

December 14, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdcfdf22-fdaf-4b07-a521-5805474f69b7

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