FDA Inspection 1120645 — KVK-Tech, Inc.

KVK-Tech, Inc. — FEI 3013676321

The FDA completed an inspection of KVK-Tech, Inc. on Mar 13, 2020 in Newtown, PA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 13, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newtown, PA (United States)