Overview
- 7 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2025-10-10.
At a glance
Inspections
7
Form 483s
1
EIRs
0
Last outcome
Clean
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 7 Oct 2025 – 10 Oct 2025 | Human Drugs | Clean | |
| 6 Aug 2024 – 9 Aug 2024 | Biologics | Clean | |
| 9 Nov 2020 – 12 Nov 2020 | Biologics | Clean | |
| 5 Mar 2015 – 11 Mar 2015 | Biologics | Clean | |
| 16 Jul 2012 | Not recorded | Clean | |
| 8 Oct 2010 | Not recorded | 483 | View 483 → |
| 11 Dec 2008 | Not recorded | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
8 Oct 2010
21 CFR 312.62(b)
Case history records- inadequate or inadequate
Cited by Nicholas C Mendiola
Investigators
FDA investigators tied to this site in the record.
Karen L Kosar3 insp.
Benton M Ketron2 insp.
Ann B Borromeo1 insp.
Nicholas C Mendiola1 insp.
Joseph J Vannelli1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 312.62(b) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Matthew G. Davis, M.D.'s 1 Form 483
Verbatim observations 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