Overview
- 3 FDA inspections are on record.
- 2 inspections produced a Form 483.
- The most recent recorded inspection date is 2026-06-11.
At a glance
Inspections
3
Form 483s
2
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 8 Jun 2026 – 11 Jun 2026 | Medical Devices & Rad Health | 483 | View 483 → |
| 6 Feb 2023 – 9 Feb 2023 | Medical Devices & Rad Health | 483 | View 483 → |
| 9 Sep 2019 – 12 Sep 2019 | Medical Devices & Rad Health | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
11 Jun 2026
ISO 13485:2016 Clause 7.1
Product realization risk management processes not documented
Cited by Matthew M Vernon
11 Jun 2026
ISO 13485:2016 Clause 7.3.1
Design and development procedures not documented
Cited by Matthew M Vernon
11 Jun 2026
ISO 13485:2016 Clause 7.3.9
Procedures to control design and development changes not documented
Cited by Matthew M Vernon
9 Feb 2023
21 CFR 820.50
Purchasing controls, Lack of or inadequate procedures
Cited by Natasha R Johnson
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 820.50 | Cited across public-safe Form 483 observations | 1x |
| ISO 13485:2016 Clause 7.1 | Cited across public-safe Form 483 observations | 1x |
| ISO 13485:2016 Clause 7.3.1 | Cited across public-safe Form 483 observations | 1x |
| ISO 13485:2016 Clause 7.3.9 | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Manatec S.A.R.L.'s 2 Form 483s
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