FDA Warning Letter — KVK-Tech, Inc.

Case 608236 — FEI 3013676321

The FDA took a Warning Letter action against KVK-Tech, Inc. on Oct 8, 2020 (Newtown, PA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
KVK-Tech, Inc.
Date
Oct 8, 2020
Fiscal Year
2021
Product Type
Drugs
Center
CDER
Location
Newtown, PA (United States)