FDA Inspection 810163 — NerPharMa S.R.L.

NerPharMa S.R.L. — FEI 3004762406

The FDA completed an inspection of NerPharMa S.R.L. on Dec 12, 2012 in Nerviano. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 12, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nerviano (Italy)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.