Charlotte P. Chang
FDA investigator
Appears on 3 documents from 2022 to 2026, mostly at sites in New Jersey. Most often cites what specifications must you establish? (21 CFR 111.70).
- 3
- Documents on file
- 14.0
- Observations per 483
- 2022
- First seen
- 2026
- Most recent
What they cite most
From 42 observations- 21 CFR 111.70What specifications must you establish?4
- 21 CFR 111.123What quality control operations are required for the master manufacturing record, the batch production record, and manufacturing operations?3
- 21 CFR 111.75What must you do to determine whether specifications are met?3
- 21 CFR 211.160General requirements3
- 21 CFR 211.194Laboratory records3
- 21 CFR 211.67Equipment cleaning and maintenance3
Activity by year
2022: 1, 2023: 1, 2026: 1
Where
New Jersey 3
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-01-27 | 483 Neeyaan LLCJan 27, 2026 · Cranbury, New Jersey | Cranbury, New Jersey | 25 | |
| 2023-07-14 | 483 Aspire Pharmaceuticals Inc.Jul 14, 2023 · Somerset, New Jersey | Somerset, New Jersey | 1 | |
| 2022-02-03 | 483 Aspire Pharmaceuticals Inc.Feb 3, 2022 · Somerset, New Jersey | Somerset, New Jersey | 16 |
About this profile
What does Charlotte P. Chang inspect?
Charlotte P. Chang appears on 3 documents on file covering 2 sites, mostly in New Jersey.
What do they cite most often?
21 CFR 111.70 (what specifications must you establish?), followed by 21 CFR 111.123 and 21 CFR 111.75.
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 Charlotte P. Chang is dated Jan 27, 2026.