FDA Inspection 810163 — NerPharMa S.r.l.

NerPharMa S.r.l. — FEI 3004762406

The FDA completed an inspection of NerPharMa S.r.l. on December 12, 2012 in Nerviano. 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 12, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nerviano (Italy)