FDA Inspection 1096555 - Avery Biomedical Devices, Inc. - July 16, 2019
FDA Inspection 1096555 for Avery Biomedical Devices, Inc. on July 16, 2019. Classification: No Action Indicated (NAI).
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FDA Inspection 1096555 for Avery Biomedical Devices, Inc. on July 16, 2019. Classification: No Action Indicated (NAI).
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Inspection Date
July 16, 2019
Product Type
Devices
ID: fa3349c0-0b72-4da1-bf39-99d078d6a011
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