Nongshim Anyang Factory FDA Record
- Latest inspection NAI · Jun 2, 2016
- No warning letters matched by name
Nongshim Anyang Factory has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Nongshim Anyang Factory" is on file.
- Latest inspection
- Jun 2, 2016 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 2 | Nov 15, 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 2, 2016 | Gunpo, Korea (The Republic Of) | Food/Cosmetics | No Action Indicated (NAI) | 3011384759 |
| Jul 26, 2011 | Gunpo-Si, Korea (The Republic Of) | Food/Cosmetics | No Action Indicated (NAI) | 3004297796 |
- 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 3011384759 | Gunpo, Korea (The Republic Of) | 1 | Jun 2, 2016 |
| FEI 3004297796 | Gunpo-Si, Korea (The Republic Of) | 1 | Jul 26, 2011 |
Nongshim Anyang Factory and the FDA: common questions
Has Nongshim Anyang Factory received an FDA warning letter?
No FDA warning letter addressed to the name "Nongshim Anyang 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 Nongshim Anyang Factory received an FDA Form 483?
FDA has not published a Form 483 for "Nongshim Anyang Factory" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Nongshim Anyang Factory?
The most recent FDA inspection on file ended Jun 2, 2016 at Gunpo, Korea (The Republic Of) and was classified NAI. FDA has 2 inspections of Nongshim Anyang Factory on file.
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