FDA Inspection 662472 — Konec Inc.

Konec Inc. — FEI 3000207081

The FDA completed an inspection of Konec Inc. on May 13, 2010 in Tucson, AZ. 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
May 13, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tucson, AZ (United States)