Overview
- 6 public-safe observations are available for this inspection.
- 6 structured CFR citations are represented.
- 2 investigators are tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
4 Oct 2012
21 CFR 820.20(c)
Management review - Lack of or inadequate procedures
Cited by Wendy R Blame, Erica M Katherine
4 Oct 2012
21 CFR 820.50(a)(3)
Acceptable supplier records, inadequate records
Cited by Wendy R Blame, Erica M Katherine
4 Oct 2012
21 CFR 820.72(a)
Equipment control activity documentation
Cited by Wendy R Blame, Erica M Katherine
4 Oct 2012
21 CFR 820.100(a)
Lack of or inadequate procedures
Cited by Wendy R Blame, Erica M Katherine
4 Oct 2012
21 CFR 820.184
DHR - not or inadequately maintained
Cited by Wendy R Blame, Erica M Katherine
Inspected site
HIHoward Instruments IncTuscaloosa, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.100(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.184 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.198(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.20(c) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.50(a)(3) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.72(a) | Cited across public-safe Form 483 observations | 1x |
Source document
PDF
PDF available
Form 483 source document
The source document is available to authorized Atlas users.
Full 483 report
Get the verbatim text of all 6 observations
The source PDF and every observation in full, so your team sees exactly what was cited and how it was answered.
- The site's full inspection history around this Form 483
- Whether these citations escalated to a warning letter
- The investigators involved and the citations they repeat elsewhere