Elwira Gromniak, MD FDA Record
Elwira Gromniak, MD has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Elwira Gromniak, MD" is on file.
- Latest inspection
- Mar 29, 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 | 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 |
|---|---|---|---|---|
| Mar 29, 2017 | Szczecin, Poland | Drugs | Voluntary Action Indicated (VAI) | 3013134981 |
- 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 3013134981 | Szczecin, Poland | 1 | Mar 29, 2017 |
Elwira Gromniak, MD and the FDA: common questions
Has Elwira Gromniak, MD received an FDA warning letter?
No FDA warning letter addressed to the name "Elwira Gromniak, MD" 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 Elwira Gromniak, MD received an FDA Form 483?
FDA has not published a Form 483 for "Elwira Gromniak, MD" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Elwira Gromniak, MD?
The most recent FDA inspection on file ended Mar 29, 2017 at Szczecin, Poland and was classified VAI. FDA has 1 inspection of Elwira Gromniak, MD on file.
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