FDA Inspection 944245 — Laboratorios Kener, SA De CV

Laboratorios Kener, SA De CV — FEI 3006763268

The FDA completed an inspection of Laboratorios Kener, SA De CV on Sep 9, 2015 in Ciudad De Mexico. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.