Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc.
FDA inspection history in Laurel, Mississippi, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Laurel, Mississippi.
Cited most
Across all Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs observations on file
- FDCA 501(a)(2)(A)Insanitary conditions4
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Laurel, Mississippi
One Form 483 · 2018 · 5 observations
Latest: Form 483, Nov 29, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-11-29 | 483 Form 483 | Laurel, Mississippi | 5 | $99 |
Investigators on these documents
FEI number 3014539091 · most recent document Nov 29, 2018
About Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc.
How many FDA Form 483s has Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc. received?
FDA Intel has 1 Form 483 on file for Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc.; the most recent is dated Nov 29, 2018.
When was Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc. is a Form 483 dated Nov 29, 2018, for the site in Laurel, Mississippi.
What did FDA cite at Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc.?
The regulations cited most in the observations on file for Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc. are FDCA 501(a)(2)(A) (Insanitary conditions), 4 times; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.