Carlton's Dunwoody Pharmacy Corp.
FDA inspection history in Dunwoody, Georgia, 2016 to 2019
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Dunwoody, Georgia.
- 2016The longest 483 on file: 5 observations over 3 pages at Dunwoody, Georgia.
- 2019One Form 483, at Dunwoody, Georgia.
Cited most
Across all Carlton's Dunwoody Pharmacy observations on file
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22(c)Responsibilities of quality control unit1
The complete Carlton's Dunwoody Pharmacy 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
Dunwoody, Georgia
Two Form 483s · 2016 to 2019 · 6 observations
Latest: Form 483, Apr 12, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-12 | 483 Form 483 | Dunwoody, Georgia | 1 | $99 |
| 2016-01-13 | 483 Form 483 | Dunwoody, Georgia | 5 | $99 |
Investigators on these documents
Tamara J. Henderson (2)Rachael L. Cook (1)Veronica Fuentes (1)
FEI number 3011755158 · most recent document Apr 12, 2019
About Carlton's Dunwoody Pharmacy Corp.
How many FDA Form 483s has Carlton's Dunwoody Pharmacy Corp. received?
FDA Intel has 2 Form 483s on file for Carlton's Dunwoody Pharmacy Corp.; the most recent is dated Apr 12, 2019.
When was Carlton's Dunwoody Pharmacy Corp. last inspected by FDA?
The most recent FDA inspection document on file for Carlton's Dunwoody Pharmacy Corp. is a Form 483 dated Apr 12, 2019, for the site in Dunwoody, Georgia.
What did FDA cite at Carlton's Dunwoody Pharmacy Corp.?
The regulations cited most in the observations on file for Carlton's Dunwoody Pharmacy Corp. are 21 CFR 211.160(b)(4) (General requirements), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.