Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3001237796.
Observations1
Issue DateMarch 18, 2022
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections10
Establishment Details
Firm
The Ritedose Corporation
Location
Columbia, South Carolina, United States
FEI Number
3001237796
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
March 18, 2022
Country
United States
Inspection History, 2010 to 2025
NAI5
VAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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