FDA Inspection 1086467 — KVK Tech, Inc.

KVK Tech, Inc. — FEI 3005117563

The FDA completed an inspection of KVK Tech, Inc. on April 16, 2019 in Newtown, PA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newtown, PA (United States)