Overview
- 16 public-safe observations are available for this inspection.
- 8 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.
21 May 2019
21 CFR 211.110(b)
In-process conformity - examination, sample testing
Cited by Cheryl A Clausen, Zhihao Pete Qiu
21 May 2019
21 CFR 211.113(b)
Procedures for sterile drug products
Cited by Cheryl A Clausen, Zhihao Pete Qiu
21 May 2019
21 CFR 211.188(b)
Batch production and Batch Control Record Requirements
Cited by Cheryl A Clausen, Zhihao Pete Qiu
21 May 2019
21 CFR 211.194(a)
Complete test data included in records
Cited by Cheryl A Clausen, Zhihao Pete Qiu
Inspected site
GPGP PHARM S.A.U.Sant Quinti De Mediona, Spain
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.100(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.110(b) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.113(b) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.188(b) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.194(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.22(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.25(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.67(a) | Cited across public-safe Form 483 observations | 2x |
Full 483 report
Get the verbatim text of all 16 observations
The full inspection record, as Atlas holds it, 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