Pharma Pac, LLC
FDA inspection history in De Kalb, Mississippi, 2019
- 2
- Form 483s
Every document, by year
- Form 483
2019: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2019Two Form 483s, at De Kalb, Mississippi.
- 2019The longest 483 on file: 6 observations over 4 pages at De Kalb, Mississippi.
Cited most
Across all Pharma Pac observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Pharma Pac file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
De Kalb, Mississippi
Two Form 483s · 2019 · 9 observations
Latest: Form 483, Aug 9, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-09 | 483 Form 483 | De Kalb, Mississippi | 6 | $99 |
| 2019-06-18 | 483 Form 483 | De Kalb, Mississippi | 3 | $99 |
Investigators on these documents
FEI number 3003982004 · most recent document Aug 9, 2019
About Pharma Pac, LLC
How many FDA Form 483s has Pharma Pac, LLC received?
FDA Intel has 2 Form 483s on file for Pharma Pac, LLC; the most recent is dated Aug 9, 2019.
When was Pharma Pac, LLC last inspected by FDA?
The most recent FDA inspection document on file for Pharma Pac, LLC is a Form 483 dated Aug 9, 2019, for the site in De Kalb, Mississippi.
What did FDA cite at Pharma Pac, LLC?
The regulations cited most in the observations on file for Pharma Pac, LLC are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.180(e)(2) (General requirements), 1 time.