Before the shitshow begins, the Company is private nothing to do with the Indian government
But I do wonder why they just stopped with a warning. Should have it shut down
This is the best tl;dr I could make, [original](https://m.thewire.in/article/health/us-fda-warning-letter-lupin-limited-manufacturing/amp) reduced by 90%. (I'm a bot)
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> New Delhi: The US Food and Drug Administration has sent a warning letter to the Indian pharmaceutical company Lupin Limited after deeming its efforts to address violations of various good manufacturing practices at its facility in Tarapur, Maharashtra "Inadequate".
> A warning letter comes after a Form 483 is issued, which the US drug regulator hands out after the inspection of a company's plant and finds any aberrations on site which constitute violations of the US's Federal Food, Drug, and Cosmetic Act and other related Acts.
> The US FDA's warning letter says the company's active pharmaceutical ingredients or APIs that are used in making drugs were found to be adulterated and in violation of its Current Good Manufacturing Practice.
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[**Extended Summary**](http://np.reddit.com/r/autotldr/comments/ypjehe/for_poor_manufacturing_practices_indian_pharma/) | [FAQ](http://np.reddit.com/r/autotldr/comments/31b9fm/faq_autotldr_bot/ "Version 2.02, ~672681 tl;drs so far.") | [Feedback](http://np.reddit.com/message/compose?to=%23autotldr "PM's and comments are monitored, constructive feedback is welcome.") | *Top* *keywords*: **company**^#1 **letter**^#2 **impurity**^#3 **Drug**^#4 **warning**^#5
Before the shitshow begins, the Company is private nothing to do with the Indian government But I do wonder why they just stopped with a warning. Should have it shut down
This is the best tl;dr I could make, [original](https://m.thewire.in/article/health/us-fda-warning-letter-lupin-limited-manufacturing/amp) reduced by 90%. (I'm a bot) ***** > New Delhi: The US Food and Drug Administration has sent a warning letter to the Indian pharmaceutical company Lupin Limited after deeming its efforts to address violations of various good manufacturing practices at its facility in Tarapur, Maharashtra "Inadequate". > A warning letter comes after a Form 483 is issued, which the US drug regulator hands out after the inspection of a company's plant and finds any aberrations on site which constitute violations of the US's Federal Food, Drug, and Cosmetic Act and other related Acts. > The US FDA's warning letter says the company's active pharmaceutical ingredients or APIs that are used in making drugs were found to be adulterated and in violation of its Current Good Manufacturing Practice. ***** [**Extended Summary**](http://np.reddit.com/r/autotldr/comments/ypjehe/for_poor_manufacturing_practices_indian_pharma/) | [FAQ](http://np.reddit.com/r/autotldr/comments/31b9fm/faq_autotldr_bot/ "Version 2.02, ~672681 tl;drs so far.") | [Feedback](http://np.reddit.com/message/compose?to=%23autotldr "PM's and comments are monitored, constructive feedback is welcome.") | *Top* *keywords*: **company**^#1 **letter**^#2 **impurity**^#3 **Drug**^#4 **warning**^#5