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FDA Inspection 737597 — KVK Tech, Inc.

KVK Tech, Inc. — FEI 3005117563

The FDA completed an inspection of KVK Tech, Inc. on August 1, 2011 in Newtown, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 1, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newtown, PA (United States)

Facility

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Recent compliance actions

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