Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3015474688.
Observations7
Issue DateJuly 03, 2019
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
RePharm LLC
Location
Riverside, Missouri, United States
FEI Number
3015474688
Product Type
Drugs
Issue Date
July 03, 2019
Country
United States
Inspection History, 2019 to 2023
VAI1
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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