FDA Inspection 914956 — IOI OLEO GMBH

IOI OLEO GMBH — FEI 3002807213

The FDA completed an inspection of IOI OLEO GMBH on Feb 27, 2015 in Witten. 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
Feb 27, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Witten (Germany)

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