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 3011853315.
Observations4
Issue DateJanuary 09, 2025
StatusNo Warning Letter
Establishment TypeSource Plasma Firm
Related Inspections2
Establishment Details
Firm
Biomat USA, Inc.
Location
Cedar City, Utah, United States
FEI Number
3011853315
Establishment Type
Source Plasma Firm
Product Type
Biologics
Issue Date
January 09, 2025
Country
United States
Inspection History, 2018 to 2025
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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