Missouri Analytical Laboratories Inc
FDA inspection history in Saint Louis, Missouri, 2021
- 1
- Warning letter
- 1
- Form 483
- 1
- Close-out
Every document, by year
- Warning letter
- Form 483
- Close-out
2021: one warning letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One warning letter and one Form 483, at Saint Louis, Missouri.
Cited most
Across all Missouri Analytical Laboratories observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.194(a)(7)Laboratory records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Missouri Analytical Laboratories file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
Saint Louis, Missouri
One warning letter, one Form 483 and one close-out letter · 2021 · 5 observations
Latest: Warning letter, Sep 30, 2021 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-09-30 | Warning letter Warning letter | Saint Louis, Missouri | — | $99 |
| 2021-05-19 | 483 Form 483 | Saint Louis, Missouri | 5 | $99 |
| Undated | Close-out Close-out letter | Saint Louis, Missouri | — | $99 |
Investigators on these documents
FEI number 1946524 · most recent document Sep 30, 2021
About Missouri Analytical Laboratories Inc
How many FDA Form 483s has Missouri Analytical Laboratories Inc received?
FDA Intel has 1 Form 483 on file for Missouri Analytical Laboratories Inc; the most recent is dated May 19, 2021.
When was Missouri Analytical Laboratories Inc last inspected by FDA?
The most recent FDA inspection document on file for Missouri Analytical Laboratories Inc is a Form 483 dated May 19, 2021, for the site in Saint Louis, Missouri.
What did FDA cite at Missouri Analytical Laboratories Inc?
The regulations cited most in the observations on file for Missouri Analytical Laboratories Inc are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.194(a)(7) (Laboratory records), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.
Has Missouri Analytical Laboratories Inc received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Missouri Analytical Laboratories Inc; the most recent is dated Sep 30, 2021.