FDA Inspection 1028813 — Emott AG

Emott AG — FEI 3009216424

The FDA completed an inspection of Emott AG on September 1, 2017 in Gockhausen. 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
September 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gockhausen (Switzerland)