Amerisource Bergen Drug Corporation
FDA Regulatory Profile
Amerisource Bergen Drug Corporation has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Mar 22, 2024 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 5 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Mar 22, 2024 | Phoenix, AZ | Food/Cosmetics | No Action Indicated (NAI) | 3004387303 |
| Sep 13, 2016 | Salt Lake City, UT | Food/Cosmetics | No Action Indicated (NAI) | 1713263 |
| Jun 23, 2016 | Phoenix, AZ | Food/Cosmetics | No Action Indicated (NAI) | 3004387303 |
| Apr 8, 2014 | Romeoville, IL | Drugs | No Action Indicated (NAI) | 3005338985 |
| Oct 7, 2008 | Des Moines, WA | Drugs | Voluntary Action Indicated (VAI) | 3021537 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.