Master Herbs, Inc
FDA inspection history in Pomona, California, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Pomona, California.
Cited most
Across all Master Herbs observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit2
- 21 CFR 211.142(b)Warehousing procedures1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Master Herbs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pomona, California
One Form 483 · 2020 · 4 observations
Latest: Form 483, Sep 14, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-09-14 | 483 Form 483 | Pomona, California | 4 | $99 |
Investigators on these documents
FEI number 3008916049 · most recent document Sep 14, 2020
About Master Herbs, Inc
How many FDA Form 483s has Master Herbs, Inc received?
FDA Intel has 1 Form 483 on file for Master Herbs, Inc; the most recent is dated Sep 14, 2020.
When was Master Herbs, Inc last inspected by FDA?
The most recent FDA inspection document on file for Master Herbs, Inc is a Form 483 dated Sep 14, 2020, for the site in Pomona, California.
What did FDA cite at Master Herbs, Inc?
The regulations cited most in the observations on file for Master Herbs, Inc are 21 CFR 211.22(a) (Responsibilities of quality control unit), 2 times; 21 CFR 211.142(b) (Warehousing procedures), 1 time; 21 CFR 211.25(a) (Personnel qualifications), 1 time.