A manufacturer of acidified foods was found to be in violation of the Acidified Foods regulations because they did not fully comply with registration and
An FDA Warning Letter was issued to a sprouting operation after inspection observations found a number of serious violations that remained uncorrected. Of high concern
A facility which processes seafood and acidified foods recently received a warning letter that followed observations from a 2023 inspection which included failure to provide
An FDA inspection of a noodle manufacturer found that the facility did not have the required food safety plan and had numerous GMP violations. Specifically
A shell egg farm and processing facility being inspected by the FDA to determine compliance to the Shell Egg Regulation (21 CFR Part 118) was
The FDA citation for lack of a food safety plan included the fact that the facility had not conducted a hazard analysis which would have
Pests and situations that could lead to pest infestations were the primary focus of an FDA warning letter sent to a refrigerated, frozen and ambient
In its inspection of a raw milk cheese manufacturer, FDA inspectors detected repeated incidence of Listeria monocytogenes (Lm) and other Listeria species in the environment
Serious violations of CGMPs and the PC Rule, along with multiple instances of Listeria species in the production environment, of an RTE bakery caused FDA
It’s not all that unusual for a firm to get a Form 483 following an FDA inspection. Occasionally when the FDA considers the firm’s response
