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 1921383.
Observations3
Issue DateFebruary 20, 2025
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections10
Establishment Details
Firm
Blendhouse Allerton,LLC
Location
Allerton, Pennsylvania, United States
FEI Number
1921383
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
February 20, 2025
Country
United States
Inspection History, 2016 to 2026
NAI7
VAI3
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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