Meridian Medical Technologies, Inc.
FDA inspection history across 2 sites, 2013
- 2
- Form 483s
Every document, by year
- Form 483
2013: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2013Two Form 483s, at Saint Louis, Kansas and Saint Louis, Missouri.
- 2013The longest 483 on file: 10 observations over 9 pages at Saint Louis, Missouri.
Cited most
Across all Meridian Medical Technologies observations on file
- 21 CFR 211.192Production record review4
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.160General requirements1
The complete Meridian Medical Technologies file.
All 2 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
Saint Louis, Kansas
One Form 483 · 2013 · 5 observations
Latest: Form 483, Oct 9, 2013 →Saint Louis, Missouri
One Form 483 · 2013 · 10 observations
Latest: Form 483, Apr 29, 2013 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2013-10-09 | 483 Form 483 | Saint Louis, Kansas | 5 | $99 |
| 2013-04-29 | 483 Form 483 | Saint Louis, Missouri | 10 | $99 |
Investigators on these documents
Anthony R. Bucks (1)Kimberly E. Pera (1)Paul G. Klepper (1)Perry Williams (1)Sherry L. Bouse (1)
FEI number 1937280 · most recent document Oct 9, 2013
About Meridian Medical Technologies, Inc.
How many FDA Form 483s has Meridian Medical Technologies, Inc. received?
FDA Intel has 2 Form 483s on file for Meridian Medical Technologies, Inc.; the most recent is dated Oct 9, 2013.
When was Meridian Medical Technologies, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Meridian Medical Technologies, Inc. is a Form 483 dated Oct 9, 2013, for the site in Saint Louis, Kansas.
What did FDA cite at Meridian Medical Technologies, Inc.?
The regulations cited most in the observations on file for Meridian Medical Technologies, Inc. are 21 CFR 211.192 (Production record review), 4 times; 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.165 (Testing and release for distribution), 2 times.