Overview
- 3 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2024-11-05.
At a glance
Inspections
3
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 29 Oct 2024 – 5 Nov 2024 | Biologics | 483 | View 483 → |
| 12 Jul 2022 | Biologics | Clean | |
| 19 Jul 2018 – 25 Jul 2018 | Biologics | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
5 Nov 2024
21 CFR 1271.160(b)(3)
Actions verified, short and long term solutions
Cited by Leslie W Gilbert, Steven D Banks, Jannet M Peroti
5 Nov 2024
21 CFR 1271.200(c)
Calibration procedures and schedules (general)
Cited by Leslie W Gilbert, Steven D Banks, Jannet M Peroti
Investigators
FDA investigators tied to this site in the record.
Leslie W Gilbert2 insp.
Steven D Banks1 insp.
Jannet M Peroti1 insp.
Jennifer L Sheehan1 insp.
Laura E Garcia1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 1271.160(b)(3) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.200(c) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Eurofins Donor & Product Testing, Inc. Atlanta's 1 Form 483
Source PDFs and recurring CFR citations, so your team knows what this site gets cited for.
- The site's full inspection history, with every Form 483 and its outcome
- Warning letters and recalls tied to the company behind it
- Whether recurring CFR citations get closed out or repeat