Northern Labs, Inc.
FDA inspection history in Manitowoc, Wisconsin, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Manitowoc, Wisconsin.
Cited most
Across all Northern Labs observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.84(d)(6)Testing and approval or rejection of components, drug product containers, and closures1
The complete Northern Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Manitowoc, Wisconsin
One Form 483 · 2025 · 2 observations
Latest: Form 483, Feb 6, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-06 | 483 Form 483 | Manitowoc, Wisconsin | 2 | $99 |
Investigators on these documents
FEI number 2121746 · most recent document Feb 6, 2025
About Northern Labs, Inc.
How many FDA Form 483s has Northern Labs, Inc. received?
FDA Intel has 1 Form 483 on file for Northern Labs, Inc.; the most recent is dated Feb 6, 2025.
When was Northern Labs, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Northern Labs, Inc. is a Form 483 dated Feb 6, 2025, for the site in Manitowoc, Wisconsin.
What did FDA cite at Northern Labs, Inc.?
The regulations cited most in the observations on file for Northern Labs, Inc. are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.84(d)(6) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.