Home » FDA Calls Out Two Manufacturers Over GMP Violations
FDA Calls Out Two Manufacturers Over GMP Violations
The FDA is accusing two companies — one a dietary supplement manufacturer and one an API maker — of committing a multitude of GMP violations.
In an April 15 letter to Pacific Nutritional, the FDA accused the company of producing four adulterated dietary supplements based on a host of GMP failures.
Those purported GMP failures included an inadequate process and master manufacturing record, failure to establish proper finished product specifications, a lack of quality control procedures and a failure to establish and follow proper laboratory control processes.
Upcoming Events
-
18Jul
-
21Oct