FDA Inspection 1089541 - The Ritedose Corporation - April 18, 2019
FDA Inspection 1089541 for The Ritedose Corporation on April 18, 2019. Classification: No Action Indicated (NAI).
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FDA Inspection 1089541 for The Ritedose Corporation on April 18, 2019. Classification: No Action Indicated (NAI).
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Company
The Ritedose CorporationInspection Date
April 18, 2019
Product Type
Drugs
ID: 2eb6871a-e581-45f6-a645-8912fc5af088
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