FDA Inspection 1108091 - Celestica Oregon, LLC. - October 25, 2019
FDA Inspection 1108091 for Celestica Oregon, LLC. on October 25, 2019. Classification: No Action Indicated (NAI).
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FDA Inspection 1108091 for Celestica Oregon, LLC. on October 25, 2019. Classification: No Action Indicated (NAI).
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Company
Celestica Oregon, LLC.Inspection Date
October 25, 2019
Product Type
Devices
ID: fdb67351-2950-4af2-bcce-583814044201
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