Beijing Sundor Laser Equipment Co. Ltd. FDA Record
Beijing Sundor Laser Equipment Co. Ltd. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Beijing Sundor Laser Equipment Co. Ltd." is on file.
- Latest inspection
- Nov 9, 2018 · NAI
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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 |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Nov 9, 2018 | Beijing, China | Devices | No Action Indicated (NAI) | 3014741352 |
- 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 3014741352 | Beijing, China | 1 | Nov 9, 2018 |
Beijing Sundor Laser Equipment Co. Ltd. and the FDA: common questions
Has Beijing Sundor Laser Equipment Co. Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Beijing Sundor Laser Equipment Co. Ltd." 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 Beijing Sundor Laser Equipment Co. Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Beijing Sundor Laser Equipment Co. Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Beijing Sundor Laser Equipment Co. Ltd.?
The most recent FDA inspection on file ended Nov 9, 2018 at Beijing, China and was classified NAI. FDA has 1 inspection of Beijing Sundor Laser Equipment Co. Ltd. on file.
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