Neogen Technologies, Inc. FDA Record
Neogen Technologies, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Neogen Technologies, Inc." is on file.
- Latest 510(k)
- Aug 21, 2003
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | 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 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K032301 | NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 | Aug 21, 2003 |
Neogen Technologies, Inc. and the FDA: common questions
Has Neogen Technologies, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Neogen Technologies, Inc." 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 Neogen Technologies, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Neogen Technologies, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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