Maria J. Lopez-Barragan
FDA investigator
Appears on 2 documents from 2017, mostly at sites in New York. Most often cites general requirements (21 CFR 211.160).
- 2
- Documents on file
- 5.5
- Observations per 483
- 2017
- First seen
- 2017
- Most recent
What they cite most
From 11 observations- 21 CFR 211.160General requirements4
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
Activity by year
2017: 2
Where
New York 1 · South Korea 1
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2017-07-25 | 483 Samsung BioLogicsJul 25, 2017 · Yeonsu-gu, South Korea | Yeonsu-gu, South Korea | 4 | |
| 2017-03-17 | 483 Wyeth Pharmaceutical Division of Wyeth Holdings LLCMar 17, 2017 · Pearl River, New York | Pearl River, New York | 7 |
About this profile
What does Maria J. Lopez-Barragan inspect?
Maria J. Lopez-Barragan appears on 2 documents on file covering 2 sites, mostly in New York.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.67 and 21 CFR 211.110.
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 Maria J. Lopez-Barragan is dated Jul 25, 2017.