FDA Inspection 1037943 — Laboratorios Liomont, S.A. de C.V.

Laboratorios Liomont, S.A. de C.V. — FEI 3003948827

The FDA completed an inspection of Laboratorios Liomont, S.A. de C.V. on December 15, 2017 in Ciudad De Mexico. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 15, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ciudad De Mexico (Mexico)