Coen Van Der Zwaan, M.D. FDA Record
Coen Van Der Zwaan, M.D. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Coen Van Der Zwaan, M.D." is on file.
- Latest inspection
- Dec 15, 2023 · NAI
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 15, 2023 | Tiel, Netherlands | Drugs | No Action Indicated (NAI) | 3029204881 |
- 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 3029204881 | Tiel, Netherlands | 1 | Dec 15, 2023 |
Coen Van Der Zwaan, M.D. and the FDA: common questions
Has Coen Van Der Zwaan, M.D. received an FDA warning letter?
No FDA warning letter addressed to the name "Coen Van Der Zwaan, M.D." 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 Coen Van Der Zwaan, M.D. received an FDA Form 483?
FDA has not published a Form 483 for "Coen Van Der Zwaan, M.D." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Coen Van Der Zwaan, M.D.?
The most recent FDA inspection on file ended Dec 15, 2023 at Tiel, Netherlands and was classified NAI. FDA has 1 inspection of Coen Van Der Zwaan, M.D. on file.
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