Brandon M. Kurjanowicz
FDA investigator
Appears on 1 document from 2023. Most often cites what must the master manufacturing record include? (21 CFR 111.210).
- 1
- Documents on file
- 2.0
- Observations per 483
- 2023
- First seen
- 2023
- Most recent
What they cite most
From 2 observations- 21 CFR 111.210What must the master manufacturing record include?1
- 21 CFR 111.260What must the batch record include?1
Activity by year
2023: 1
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2023-04-20 | 483 Life Science Nutritionals Inc.Apr 20, 2023 | — | 2 |
About this profile
What does Brandon M. Kurjanowicz inspect?
Brandon M. Kurjanowicz appears on 1 document on file.
What do they cite most often?
21 CFR 111.210 (what must the master manufacturing record include?), followed by 21 CFR 111.260.
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 Brandon M. Kurjanowicz is dated Apr 20, 2023.