Nutri-Dyn Midwest, Inc
FDA inspection history in Maple Plain, Minnesota, 2015 to 2017
- 1
- Close-out
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Close-out
- Warning letter
- Form 483
2015: one Form 483; 2016: one warning letter; 2017: one close-out letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2015–17One Form 483, one warning letter and one close-out letter, at Maple Plain, Minnesota.
Cited most
Across all Nutri-Dyn Midwest observations on file
- 21 CFR 111.560(a)(1)What requirements apply to the review and investigation of a product complaint?1
- 21 CFR 111.70(e)What specifications must you establish?1
- 21 CFR 111.77(a)What must you do if established specifications are not met?1
- FDCA 761(b)(1)1
The complete Nutri-Dyn Midwest file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Maple Plain, Minnesota
One close-out letter, one warning letter and one Form 483 · 2015 to 2017 · 4 observations
Latest: Close-out, Mar 15, 2017 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-03-15 | Close-out Close-out letter | Maple Plain, Minnesota | — | $99 |
| 2016-01-15 | Warning letter Warning letter | Maple Plain, Minnesota | — | $99 |
| 2015-04-10 | 483 Form 483 | Maple Plain, Minnesota | 4 | $99 |
Investigators on these documents
FEI number 2126636 · most recent document Mar 15, 2017
About Nutri-Dyn Midwest, Inc
How many FDA Form 483s has Nutri-Dyn Midwest, Inc received?
FDA Intel has 1 Form 483 on file for Nutri-Dyn Midwest, Inc; the most recent is dated Apr 10, 2015.
When was Nutri-Dyn Midwest, Inc last inspected by FDA?
The most recent FDA inspection document on file for Nutri-Dyn Midwest, Inc is a Form 483 dated Apr 10, 2015, for the site in Maple Plain, Minnesota.
What did FDA cite at Nutri-Dyn Midwest, Inc?
The regulations cited most in the observations on file for Nutri-Dyn Midwest, Inc are 21 CFR 111.560(a)(1) (What requirements apply to the review and investigation of a product complaint?), 1 time; 21 CFR 111.70(e) (What specifications must you establish?), 1 time; 21 CFR 111.77(a) (What must you do if established specifications are not met?), 1 time.
Has Nutri-Dyn Midwest, Inc received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Nutri-Dyn Midwest, Inc; the most recent is dated Jan 15, 2016.