Medspira, Lie
FDA inspection history in Minneapolis, Minnesota, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Minneapolis, Minnesota.
Cited most
Across all Medspira, Lie observations on file
- 21 CFR 8201
- 21 CFR 820.30(j)Design controls1
The complete Medspira, Lie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Minneapolis, Minnesota
One Form 483 · 2024 · 1 observation
Latest: Form 483, Jan 16, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-16 | 483 Form 483 | Minneapolis, Minnesota | 1 | $99 |
Investigators on these documents
FEI number 3008414621 · most recent document Jan 16, 2024
About Medspira, Lie
How many FDA Form 483s has Medspira, Lie received?
FDA Intel has 1 Form 483 on file for Medspira, Lie; the most recent is dated Jan 16, 2024.
When was Medspira, Lie last inspected by FDA?
The most recent FDA inspection document on file for Medspira, Lie is a Form 483 dated Jan 16, 2024, for the site in Minneapolis, Minnesota.
What did FDA cite at Medspira, Lie?
The regulations cited most in the observations on file for Medspira, Lie are 21 CFR 820, 1 time; 21 CFR 820.30(j) (Design controls), 1 time.