FDA Inspection
KVK Tech, Inc.KVK Tech, Inc. – FDA Inspection, Sep 21, 2018
Record Details
This FDA Inspection record concerns KVK Tech, Inc., with an inspection on September 21, 2018, issued by the Philadelphia District Office, covering human drugs.
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ID · a451720f-6227-4e96-b2a1-abc0c8313055
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1066645
- FDA center
- Human Drugs
- Project area
- Generic Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.63Equipment Design, Size and Location
Full citation text and observation details available on the Dashboard.
Other FDA inspections of KVK Tech, Inc.
14| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2026 | Not classified | Philadelphia District Office | Drug Quality Assurance |
| March 14, 2025 | OAI | Philadelphia District Office | Drug Quality Assurance |
| October 21, 2024 | Not classified | Philadelphia District Office | |
| July 8, 2022 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 16, 2019 | OAI | Center for Drug Evaluation and Research | Generic Drug Evaluation |
Other documents for KVK Tech, Inc.
- FDA Inspection 1329488 - 2026-08-04
- FDA Inspection 1233334 - 2025-03-14
- FDA Inspection 1229759 - 2024-10-21
- FDA Inspection 1175552 - 2022-07-08
- FDA Inspection 1086467 - 2019-04-16
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