Overview
- 4 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2023-03-21.
At a glance
Inspections
4
Form 483s
1
EIRs
0
Last outcome
Clean
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 21 Mar 2023 | Medical Devices & Rad Health | Clean | |
| 5 Apr 2017 – 6 Apr 2017 | Medical Devices & Rad Health | Clean | |
| 28 Oct 2013 – 29 Oct 2013 | Medical Devices & Rad Health | Clean | |
| 5 May 2011 | Not recorded | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
5 May 2011
21 CFR 820.20(a)
Management ensuring quality policy is understood
Cited by Yehualashe A Gessesse
5 May 2011
21 CFR 820.70(a)
Process control procedures, Lack of or inadequate procedures
Cited by Yehualashe A Gessesse
Investigators
FDA investigators tied to this site in the record.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.20(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.30(c) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.50(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.70(a) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Daily Medical Products, Inc.'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