Ou Olivia Ma
FDA investigator
Appears on 3 documents from 2024 to 2025, mostly at sites in Tennessee. Most often cites control of microbiological contamination (21 CFR 211.113).
- 3
- Documents on file
- 4.0
- Observations per 483
- 2024
- First seen
- 2025
- Most recent
What they cite most
From 12 observations- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.192Production record review3
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures3
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.167Special testing requirements1
- 21 CFR 211.180General requirements1
Activity by year
2024: 2, 2025: 1
Where
Tennessee 2 · Maryland 1
Often inspects with
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Inspection history
3 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 | |
| 2024-10-11 | 483 Charles River Laboratories, Inc.Oct 11, 2024 · Memphis, Tennessee | Memphis, Tennessee | 3 | |
| 2024-10-11 | 483 Charles River Laboratories, IncOct 11, 2024 · Memphis, Tennessee | Memphis, Tennessee | 3 |
About this profile
What does Ou Olivia Ma inspect?
Ou Olivia Ma appears on 3 documents on file covering 2 sites, mostly in Tennessee.
What do they cite most often?
21 CFR 211.113 (control of microbiological contamination), followed by 21 CFR 211.192 and 21 CFR 211.84.
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 Ou Olivia Ma is dated Apr 28, 2025.