Overview
- 5 public-safe observations are available for this inspection.
- 5 structured CFR citations are represented.
- 1 investigator is tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
12 Apr 2024
21 CFR 1271.47(a)
Testing, screening, donor eligibility procedures
Cited by Barbara T Carmichael
12 Apr 2024
21 CFR 1271.50(a)
Determination based on screening and testing
Cited by Barbara T Carmichael
12 Apr 2024
21 CFR 1271.55(b)(2)
Listing and interpretation of CD tests performed
Cited by Barbara T Carmichael
12 Apr 2024
21 CFR 1271.65(b)(2)
Labeled re: biohazard, risks, test results
Cited by Barbara T Carmichael
Inspected site
NFNorth Florida Reproductive Biology LaboratoryJacksonville, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 1271.47(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.50(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.55(b)(1) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.55(b)(2) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.65(b)(2) | 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 5 observations
The source PDF, 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