Ana Maria Moreira De Aquino FDA Record
- Latest inspection VAI · Jul 13, 2023
- No warning letters matched by name
Ana Maria Moreira De Aquino has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Ana Maria Moreira De Aquino" is on file.
- Latest inspection
- Jul 13, 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 |
|---|---|---|---|---|
| Jul 13, 2023 | Vinhedo, Brazil | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3012302027 |
- 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 3012302027 | Vinhedo, Brazil | 1 | Jul 13, 2023 |
Ana Maria Moreira De Aquino and the FDA: common questions
Has Ana Maria Moreira De Aquino received an FDA warning letter?
No FDA warning letter addressed to the name "Ana Maria Moreira De Aquino" 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 Ana Maria Moreira De Aquino received an FDA Form 483?
FDA has not published a Form 483 for "Ana Maria Moreira De Aquino" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Ana Maria Moreira De Aquino?
The most recent FDA inspection on file ended Jul 13, 2023 at Vinhedo, Brazil and was classified VAI. FDA has 1 inspection of Ana Maria Moreira De Aquino on file.
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