All Pharma, LLC
FDA inspection history in Hialeah, Florida, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Hialeah, Florida.
Cited most
Across all All Pharma observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.65(a)Equipment construction1
- 21 CFR 211.84(a)Testing and approval or rejection of components, drug product containers, and closures1
The complete All Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Hialeah, Florida
One Form 483 · 2019 · 5 observations
Latest: Form 483, Nov 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-15 | 483 Form 483 | Hialeah, Florida | 5 | $99 |
Investigators on these documents
FEI number 3010047167 · most recent document Nov 15, 2019
About All Pharma, LLC
How many FDA Form 483s has All Pharma, LLC received?
FDA Intel has 1 Form 483 on file for All Pharma, LLC; the most recent is dated Nov 15, 2019.
When was All Pharma, LLC last inspected by FDA?
The most recent FDA inspection document on file for All Pharma, LLC is a Form 483 dated Nov 15, 2019, for the site in Hialeah, Florida.
What did FDA cite at All Pharma, LLC?
The regulations cited most in the observations on file for All Pharma, LLC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.