# KVK Tech, Inc. – FDA Inspection, Sep 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/kvk-tech-inc/a451720f-6227-4e96-b2a1-abc0c8313055
Source feed: FDA_Inspections

> FDA inspection 1066645 of KVK Tech, Inc., September 21, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 14 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066645
- Company Name: KVK Tech, Inc.
- Inspection Date: 2018-09-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Generic Drug Evaluation
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Philadelphia District Office
- Citation Count: 1

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/junho-pak/4abe53fb-ad20-490d-9e71-6216a9f863f5)

Company: https://www.keypedia.com/companies/kvk-tech-inc/f8ea60fc-cfc0-4769-8e62-a677abd59cb9

Office: https://www.keypedia.com/offices/philadelphia-district-office/c5ec7398-b3d5-4125-9793-fb7b972578d8