Overview
- 3 public-safe observations are available for this inspection.
- 3 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.
28 Jul 2023
21 CFR 211.110(a)
Control procedures to monitor and validate performance
Cited by Laura S Huffman, Jacob G Lutz
28 Jul 2023
21 CFR 211.113(b)
Validation lacking for sterile drug products
Cited by Laura S Huffman, Jacob G Lutz
28 Jul 2023
21 CFR 211.188(b)
Batch production and Batch Control Record Requirements
Cited by Laura S Huffman, Jacob G Lutz
Inspected site
ZMZoetis Manufacturing & Research Spain, S.L.La Vall De Bianya, Spain
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.110(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.113(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.188(b) | 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 3 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