Alifiya H. Ghadiali
FDA investigator
Appears on 2 documents from 2024 to 2025, mostly at sites in Maryland. Most often cites responsibilities of quality control unit (21 CFR 211.22).
- 2
- Documents on file
- 4.0
- Observations per 483
- 2024
- First seen
- 2025
- Most recent
What they cite most
From 11 observations- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.25Personnel qualifications2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.167Special testing requirements1
- 21 CFR 211.180General requirements1
- 21 CFR 211.192Production record review1
Activity by year
2024: 1, 2025: 1
Where
Maryland 1 · North Carolina 1
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2025-04-28 | 483 FDA Form 483 Catalent Harmans April 2025Apr 28, 2025 · Harmans, Maryland | Harmans, Maryland | 6 | |
| 2024-04-05 | 483 Humacyte Global, IncApr 5, 2024 · Durham, North Carolina | Durham, North Carolina | 2 |
About this profile
What does Alifiya H. Ghadiali inspect?
Alifiya H. Ghadiali appears on 2 documents on file covering 2 sites, mostly in Maryland.
What do they cite most often?
21 CFR 211.22 (responsibilities of quality control unit), followed by 21 CFR 211.25 and 21 CFR 211.113.
Can I read the observations?
Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.
How current is this profile?
The most recent document on file for Alifiya H. Ghadiali is dated Apr 28, 2025.