ILHWA CO., LTD. CHUNCHEON FACTORY FDA Record
ILHWA CO., LTD. CHUNCHEON FACTORY has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "ILHWA CO., LTD. CHUNCHEON FACTORY" is on file.
- Latest inspection
- Jun 29, 2023 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jun 29, 2023 | Chuncheon, Korea (The Republic Of) | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3012368571 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3012368571 | Chuncheon, Korea (The Republic Of) | 1 | Jun 29, 2023 |
ILHWA CO., LTD. CHUNCHEON FACTORY and the FDA: common questions
Has ILHWA CO., LTD. CHUNCHEON FACTORY received an FDA warning letter?
No FDA warning letter addressed to the name "ILHWA CO., LTD. CHUNCHEON FACTORY" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has ILHWA CO., LTD. CHUNCHEON FACTORY received an FDA Form 483?
FDA has not published a Form 483 for "ILHWA CO., LTD. CHUNCHEON FACTORY" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect ILHWA CO., LTD. CHUNCHEON FACTORY?
The most recent FDA inspection on file ended Jun 29, 2023 at Chuncheon, Korea (The Republic Of) and was classified VAI. FDA has 1 inspection of ILHWA CO., LTD. CHUNCHEON FACTORY on file.
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