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
Spice Importer Failed to Comply with FSVP Requirements; FSVP requires that importers identify and evaluate known or reasonably foreseeable hazards for each type of imported food to determine if there are any that require a preventive control. …
FDA Warning letter was received by an RTE Bakery with deficiencies in Pests and Facility Registration …
