Diamond Drugs, Inc.
FDA inspection history in Indiana, Pennsylvania, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Indiana, Pennsylvania.
Cited most
Across all Diamond Drugs observations on file
- 21 CFR 211.113Control of microbiological contamination2
The complete Diamond Drugs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Indiana, Pennsylvania
One Form 483 · 2017 · 2 observations
Latest: Form 483, Jul 21, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-07-21 | 483 Form 483 | Indiana, Pennsylvania | 2 | $99 |
Investigators on these documents
FEI number 3013075945 · most recent document Jul 21, 2017
About Diamond Drugs, Inc.
How many FDA Form 483s has Diamond Drugs, Inc. received?
FDA Intel has 1 Form 483 on file for Diamond Drugs, Inc.; the most recent is dated Jul 21, 2017.
When was Diamond Drugs, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Diamond Drugs, Inc. is a Form 483 dated Jul 21, 2017, for the site in Indiana, Pennsylvania.
What did FDA cite at Diamond Drugs, Inc.?
The regulations cited most in the observations on file for Diamond Drugs, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 2 times.