Pharmaloz Manufacturing, Inc.
FDA inspection history in Lebanon, Pennsylvania, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Lebanon, Pennsylvania.
Cited most
Across all Pharmaloz Manufacturing observations on file
- 21 CFR 211.194(a)(4)Laboratory records2
- 21 CFR 211.101(d)Charge-in of components1
- 21 CFR 211.142(b)Warehousing procedures1
- 21 CFR 211.192Production record review1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Pharmaloz Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lebanon, Pennsylvania
One Form 483 · 2018 · 6 observations
Latest: Form 483, Jun 21, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-06-21 | 483 Form 483 | Lebanon, Pennsylvania | 6 | $99 |
Investigators on these documents
FEI number 2523447 · most recent document Jun 21, 2018
About Pharmaloz Manufacturing, Inc.
How many FDA Form 483s has Pharmaloz Manufacturing, Inc. received?
FDA Intel has 1 Form 483 on file for Pharmaloz Manufacturing, Inc.; the most recent is dated Jun 21, 2018.
When was Pharmaloz Manufacturing, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Pharmaloz Manufacturing, Inc. is a Form 483 dated Jun 21, 2018, for the site in Lebanon, Pennsylvania.
What did FDA cite at Pharmaloz Manufacturing, Inc.?
The regulations cited most in the observations on file for Pharmaloz Manufacturing, Inc. are 21 CFR 211.194(a)(4) (Laboratory records), 2 times; 21 CFR 211.101(d) (Charge-in of components), 1 time; 21 CFR 211.142(b) (Warehousing procedures), 1 time.