Marissa S. Steinhagen
FDA investigator
Appears on 3 documents from 2016 to 2019, mostly at sites in Minnesota. Most often cites production and process controls (21 CFR 820.70(a)).
- 3
- Documents on file
- 2.0
- Observations per 483
- 2016
- First seen
- 2019
- Most recent
What they cite most
From 6 observations- 21 CFR 820.70(a)Production and process controls2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.30(i)Design controls1
- 21 CFR 820.80(b)Receiving, in-process, and finished device acceptance1
Activity by year
2016: 1, 2017: 1, 2019: 1
Where
Minnesota 3
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2019-05-16 | 483 Vasamed, IncMay 16, 2019 · Eden Prairie, Minnesota | Eden Prairie, Minnesota | 2 | |
| 2017-01-04 | 483 Augustine Biomedical & Design, LLC 7656 w 78th stJan 4, 2017 · Bloomington, Minnesota | Bloomington, Minnesota | 1 | |
| 2016-07-06 | 483 Synergy Health Outsourcing Solutions IncJul 6, 2016 · Maple Grove, Minnesota | Maple Grove, Minnesota | 3 |
About this profile
What does Marissa S. Steinhagen inspect?
Marissa S. Steinhagen appears on 3 documents on file covering 3 sites, mostly in Minnesota.
What do they cite most often?
21 CFR 820.70(a) (production and process controls), followed by 21 CFR 820.100(a) and 21 CFR 820.198(a).
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 Marissa S. Steinhagen is dated May 16, 2019.