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 3016710945.
Observations5
Issue DateAugust 06, 2021
Status1 Related Warning Letter
Establishment TypeProducer of Sterile and Non Sterile Drug Products
Related Inspections3
Establishment Details
Firm
Revive Rx, LLC dba Revive Rx Pharmacy
Location
Houston, Texas, United States
FEI Number
3016710945
Establishment Type
Producer of Sterile and Non Sterile Drug Products
Product Type
Drugs
Issue Date
August 06, 2021
Country
United States
Inspection History, 2021 to 2025
VAI1
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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