Siedlerstraße 7 | 68623 Lampertheim, Germany

info@zamann-pharma.com

Auriga Research Pvt. Ltd. has received an FDA Warning Letter after a February 2026 inspection of its contract testing laboratory in Bengaluru, India. FDA cited significant CGMP violations involving incomplete laboratory records, weak Quality Unit oversight, and OOS investigations based
The U.S. Food and Drug Administration (FDA) has issued a Warning Letter to ABS Corporation, a veterinary drug manufacturer in Omaha, Nebraska, after a January 2026 inspection identified significant CGMP violations involving OOS investigations, incoming component testing, and process validation.