Productos Oriente, C. Por A. FDA Record
Productos Oriente, C. Por A. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Productos Oriente, C. Por A." is on file.
- Latest inspection
- Dec 9, 2016 · 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 |
|---|---|---|---|---|
| Dec 9, 2016 | Santo Domingo, Dominican Republic (The) | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3010144229 |
- 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 3010144229 | Santo Domingo, Dominican Republic (The) | 1 | Dec 9, 2016 |
Productos Oriente, C. Por A. and the FDA: common questions
Has Productos Oriente, C. Por A. received an FDA warning letter?
No FDA warning letter addressed to the name "Productos Oriente, C. Por A." 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 Productos Oriente, C. Por A. received an FDA Form 483?
FDA has not published a Form 483 for "Productos Oriente, C. Por A." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Productos Oriente, C. Por A.?
The most recent FDA inspection on file ended Dec 9, 2016 at Santo Domingo, Dominican Republic (The) and was classified VAI. FDA has 1 inspection of Productos Oriente, C. Por A. on file.
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