PT. Muria Bahari Indonesia FDA Record
PT. Muria Bahari Indonesia has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "PT. Muria Bahari Indonesia" is on file.
- Latest inspection
- Jul 18, 2017 · 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 | 2 | 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 18, 2017 | Kudus, Indonesia | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011280608 |
| Aug 19, 2015 | Kudus, Indonesia | Food/Cosmetics | Official Action Indicated (OAI) | 3011280608 |
- 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 3011280608 | Kudus, Indonesia | 2 | Jul 18, 2017 |
PT. Muria Bahari Indonesia and the FDA: common questions
Has PT. Muria Bahari Indonesia received an FDA warning letter?
No FDA warning letter addressed to the name "PT. Muria Bahari Indonesia" 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 PT. Muria Bahari Indonesia received an FDA Form 483?
FDA has not published a Form 483 for "PT. Muria Bahari Indonesia" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect PT. Muria Bahari Indonesia?
The most recent FDA inspection on file ended Jul 18, 2017 at Kudus, Indonesia and was classified VAI. FDA has 2 inspections of PT. Muria Bahari Indonesia on file, 1 of them classified OAI (official action indicated).
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