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Published on
October 30, 2024
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KVK-Tech Warning Letters: A Timeline of Regulatory Assessments

KVK-Tech Warning Letters: A Timeline of Regulatory Assessments

Published on
October 30, 2024
Category
Written by

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Regular posts covering guidance changes, inspection findings, data methodology, and Redica product updates.

FDA issued KVK-Tech, Inc (Newtown, PA) a Warning Letter on October 8, 2020, based on the outcome of an inspection ending March 13, 2020 (Link to the corresponding FDA 483). Additionally, the firm had also received a Warning Letter on February 11, 2020, based on the outcome of an inspection ending April 16, 2019 (Link to the corresponding FDA 483)

KVK-Tech is identified as a drug packaging operation. In the October Warning Letter, FDA noted that similar GMP violations have been identified at other facilities owned by the firm, but did not reference the Warning Letter from February. “These repeated failures at multiple sites demonstrate that management oversight and control over the manufacture of drugs is inadequate”

This document illustrates the chronology of the documentation arising as an outcome to the inspections across sites for KVK-Tech in the past few years:

KVK-TECH, INC - Form 483, 2022-07-12

Document Type FDA 483
Inspection Duration July, 2022 - July, 2022
Site KVK-TECH, INC [Newtown / United States of America]
FEI 3005117563
Investigator(s) Jose M Cayuela, Monika Borkowska, Saleem A Akhtar
Redica ID 100027600
Purchase Link Purchase KVK-TECH, INC - Form 483, 2022-07-12

KVK-TECH, INC - Form 483, 2022-07-12 Snapshot

KVK-TECH, INC - Form 483, 2021-06-11

KVK-TECH, INC - Form 483, 2021-06-11 Snapshot

KVK-TECH, INC - Form 483, 2020-03-13

Document Type:FDA 483Inspection Duration:March, 2020 - March, 2020Site:KVK-TECH, INC [Newtown / United States of America]FEI:3013676321Investigator(s):Nancy M Espinal, Michele GottshallRedica ID:100111525Purchase LinkPurchase KVK-TECH, INC - Form 483, 2020-03-13

KVK-TECH, INC - Form 483, 2020-03-13 Snapshot

KVK-TECH, INC - Form 483, 2019-04-16

Document Type:FDA 483Inspection Duration:April, 2019 - April, 2019Site:KVK-TECH, INC [Newtown / United States of America]FEI:3005117563Investigator(s):Yvesna C Blaise, Nicholas A Violand, Michael R Klapal, Patrick C KlotzbuecherRedica ID:100144021Purchase LinkPurchase KVK-TECH, INC - Form 483, 2019-04-16

KVK-TECH, INC - Form 483, 2019-04-16 Snapshot

KVK-TECH, INC - Form 483, 2018-09-21

Document Type:FDA 483Inspection Duration:September, 2018 - September, 2018Site:KVK-TECH, INC [Newtown / United States of America]FEI:3005117563Investigator(s):Junho Pak, Anastasia I OffordileRedica ID:100139042Purchase LinkPurchase KVK-TECH, INC - Form 483, 2018-09-21

KVK-TECH, INC - Form 483, 2018-09-21 Snapshot

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