Hai Minh FDA Record
Hai Minh has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Hai Minh" is on file.
- Latest inspection
- Feb 25, 2020 · 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 |
|---|---|---|---|---|
| Feb 25, 2020 | Cu Chi District, Vietnam | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3010060414 |
- 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 3010060414 | Cu Chi District, Vietnam | 1 | Feb 25, 2020 |
Hai Minh and the FDA: common questions
Has Hai Minh received an FDA warning letter?
No FDA warning letter addressed to the name "Hai Minh" 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 Hai Minh received an FDA Form 483?
FDA has not published a Form 483 for "Hai Minh" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Hai Minh?
The most recent FDA inspection on file ended Feb 25, 2020 at Cu Chi District, Vietnam and was classified VAI. FDA has 1 inspection of Hai Minh on file.
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