FDA Inspection 872188 — MEDA Manufacturing GmbH

MEDA Manufacturing GmbH — FEI 3002808393

The FDA completed an inspection of MEDA Manufacturing GmbH on Nov 22, 2013 in Cologne. 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
Nov 22, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cologne (Germany)

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