Antonio Manuel Garrido Hermosilla, M.D. FDA Record
Antonio Manuel Garrido Hermosilla, M.D. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Antonio Manuel Garrido Hermosilla, M.D." is on file.
- Latest inspection
- Sep 18, 2026 · 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 |
|---|---|---|---|---|
| Sep 18, 2026 | Sevilla, Spain | Drugs | Voluntary Action Indicated (VAI) | 3044760911 |
- 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 3044760911 | Sevilla, Spain | 1 | Sep 18, 2026 |
Antonio Manuel Garrido Hermosilla, M.D. and the FDA: common questions
Has Antonio Manuel Garrido Hermosilla, M.D. received an FDA warning letter?
No FDA warning letter addressed to the name "Antonio Manuel Garrido Hermosilla, 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 Antonio Manuel Garrido Hermosilla, M.D. received an FDA Form 483?
FDA has not published a Form 483 for "Antonio Manuel Garrido Hermosilla, M.D." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Antonio Manuel Garrido Hermosilla, M.D.?
The most recent FDA inspection on file ended Sep 18, 2026 at Sevilla, Spain and was classified VAI. FDA has 1 inspection of Antonio Manuel Garrido Hermosilla, M.D. on file.
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