Overview
- 1 FDA inspection is on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2023-06-28.
At a glance
Inspections
1
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 26 Jun 2023 – 28 Jun 2023 | Medical Devices & Rad Health | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
28 Jun 2023
21 CFR 820.50
Purchasing controls, Lack of or inadequate procedures
Cited by Karen M Rodriguez, Karen M Cruz Arenas
28 Jun 2023
21 CFR 820.70(b)
Production and Process Change Procedures, lack of or Inad.
Cited by Karen M Rodriguez, Karen M Cruz Arenas
Investigators
FDA investigators tied to this site in the record.
Karen M Rodriguez1 insp.
Karen M Cruz Arenas1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.50 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.70(b) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Boyd Technologies (Thailand) Co., Ltd.'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