Overview
- 1 public-safe observation is available for this inspection.
- 1 structured CFR citation is represented.
- 3 investigators are tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
10 Mar 2009
21 CFR 211.113(b)
Validation lacking for sterile drug products
Cited by Paul L Bellamy, Devon Jenkins, Krystyna M Kitson
Inspected site
HPHikma Pharmaceuticals USA Inc.Cherry Hill, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.113(b) | Cited across public-safe Form 483 observations | 1x |
Full 483 report
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- 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