CFAI
C.F.A.I.
Government Data Intelligence Services

USPlabs, LLC

Company TX
Found in 2 federal databases · 7 total records
Department of Justice 1 records
DOJ: USPlabs and Corporate Officers Indicted 2015-11-17
DALLAS — An 11-count indictment has been unsealed today against USPlabs LLC, a Dallas firm that formerly manufactured highly popular workout and weight loss supplements. The indictment charges USPlabs...
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fda 6 records
FDA Recall: USPlabs, LLC — Class I 20140122
USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegel | Product: USPlabs OxyELITE Pro Super Thermo POWD...
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FDA Food Recall: USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport Syste 2014-01-22
Class I — USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse ...
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FDA Food Recall: USPlabs OxyELITE Pro Super Thermo DIETARY SUPPLEMENT Manufactured for USPlabs, L 2014-01-22
Class I — USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse ...
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FDA Food Recall: USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport Syste 2014-01-22
Class I — USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse ...
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FDA Food Recall: USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport Syste 2014-01-22
Class I — USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse ...
View Source
FDA Food Recall: USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport Syste 2014-01-22
Class I — USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse ...
View Source
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