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FDA Inspection 835663 — The Ritedose Corporation

The Ritedose Corporation — FEI 3001237796

The FDA completed an inspection of The Ritedose Corporation on November 8, 2012 in Columbia, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 8, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Columbia, SC (United States)

Facility

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