FDA Inspection 1302726 - Rejoni, Inc. - February 09, 2026
FDA Inspection 1302726 for Rejoni, Inc. on February 09, 2026. Classification: No Action Indicated (NAI).
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FDA Inspection 1302726 for Rejoni, Inc. on February 09, 2026. Classification: No Action Indicated (NAI).
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Company
Rejoni, Inc.Inspection Date
February 9, 2026
Product Type
Devices
ID: f8899e71-ffa2-491e-8e28-90cad6e77e7a
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