FDA Inspection 571572 — PDM Acondifarma, S.A. De C.V.

PDM Acondifarma, S.A. De C.V. — FEI 3002815808

The FDA completed an inspection of PDM Acondifarma, S.A. De C.V. on Jan 21, 2009 in Ramos Arizpe. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 21, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ramos Arizpe (Mexico)