FDA Inspection Report Cited 20 Violations for J&J

Published On: May 27th, 2010

Today J&J faces scrutiny from the House Committee on Oversight and Government Reform.

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FDA Inspection Report Cited 20 Violations for J&J

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2012-02-11T02:51:37Z - Reply - View Tweet
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2012-02-11T02:51:22Z - Reply - View Tweet
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2012-02-11T02:51:15Z - Reply - View Tweet
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2012-02-11T02:51:12Z - Reply - View Tweet
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2012-02-11T02:51:06Z - Reply - View Tweet
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2012-02-11T02:51:02Z - Reply - View Tweet
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After FDA Warning, J&J Yanks Online Video for Pain Med
In the latest sign that drug marketers continue to struggle with advertising rules in the online world, the FDA sent this warning letter to J&J, advising the company that an online video for its pain drug Ultram ER “omits and minimzed the serious risks of the drug.” The letter also says the video claims benefits..
FDA Isn’t Ready to Approve J&J Anticlotting Drug
Despite a 15-2 vote by an advisory panel in favor of the experimental anticlotting drug rivaroxaban, the FDA isn’t approving the drug at this point. ..
A.M. Vitals: More Light Shed on J&J, FDA Communication
In the Loop: J&J says it kept the FDA informed of its plan to quietly remove defective Motrin from the shelves rather than carry out a recall, according to correspondence between the company and an FDA official, the WSJ reports. However, the FDA says it wasn’t aware of the efforts ..
FDA Identifies More Problems at J&J Plant
A J&J spokesman says the company will “quickly provide a detailed response to the FDA and work to address these most recent observations.” ..
FDA Commissioner: Use Generic Alternatives to Recalled J&J Meds
Yesterday the FDA said that an April inspection of the problematic plant had turned up raw materials contaminated by certain bacteria that may cause infections. ..
J&J Gets Grilled: FDA Weighs Criminal Penalties Over Manufacturing
The FDA might seek criminal penalties against J&J’s McNeil Consumer Healthcare unit due to its “pattern of noncompliance” with good manufacturing practices. ..

Orshe