FDA 483, dated June 11, 2008, (9 pages)
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Modern Warrior Recalls “Modern Warrior Ready” Dietary Supplement Due to Undeclared 1,4-DMAA and Aniracetam, as Well as Tianeptine, Which has Not Been Approved for Supplement Use by the FDA.
[Phoenix, Arizona] – [12/22/25] – Modern Warrior is voluntarily recalling all lots of Modern Warrior Ready, a dietary supplement sold directly to consumers, after regulatory testing identified the presence of undeclared ingredients, including tianeptine, 1,4-DMAA, and aniracetam..Tianeptine can cQualgen LLC. Edmond, OK. 483 issued 09/04/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 09/04/2025
Short Title (70 char) Qualgen LLC. Edmond, OK. 483 issued 09/04/2025
FEI Number 3011286349
Firm Name Qualgen LLC
Record Type 483
State OK
Establishment Type Outsourcing FacilityGeneric Drug User Fee Amendments
FDA is soliciting general comments on GDUFA II Program Fee: List of Abbreviated New Drug Application Sponsors and Application Numbers. The information gathered from public comments will assist FDA in accurately assessing FY 2018 GDUFA Program Fees in a timely manner.Pacific International Marketing Recalls Fresh Italian Parsley Because of Possible Health Risk
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