FDA Inspection 990174 — Mylan Pharmaceuticals Inc.

Mylan Pharmaceuticals Inc. — FEI 3007886374

The FDA completed an inspection of Mylan Pharmaceuticals Inc. on October 14, 2016 in San Carlos, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 14, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
San Carlos, CA (United States)