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Agency says company released multiple batches of products to the US market without adequate testing of zinc oxide and titanium dioxide content.
June 8, 2023
By: Christine Esposito
Editor-in-Chief
The US Food and Drug Administration (FDA) has sent a warning letter for violations of CGMP regulations to Mr. Lulu LLC, a California-based company. The June 1, 2023 letter, which addressed to Roi Chairat, came after the agency conducted an inspection of the company’s manufacturing facility in Claremont, CA between November 30 and December 9, 2022. The warning letter summarizes significant violations of Current Good Manufacturing Practice (CGMP) regulations for finished pharmaceuticals. ...
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