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FDA Inspection 1065833 — Mylan Technologies Inc.

Mylan Technologies Inc. — FEI 1220747

The FDA completed an inspection of Mylan Technologies Inc. on August 15, 2018 in Saint Albans, VT. 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
August 15, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Albans, VT (United States)

Facility

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FDA data resources