Renu Laboratories, LLC
FDA inspection history in Warminster, Pennsylvania, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Warminster, Pennsylvania.
Cited most
Across all Renu Laboratories observations on file
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.198(a)Complaint files1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Renu Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Warminster, Pennsylvania
One Form 483 · 2022 · 7 observations
Latest: Form 483, Jul 27, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-07-27 | 483 Form 483 | Warminster, Pennsylvania | 7 | $99 |
Investigators on these documents
FEI number 3003263206 · most recent document Jul 27, 2022
About Renu Laboratories, LLC
How many FDA Form 483s has Renu Laboratories, LLC received?
FDA Intel has 1 Form 483 on file for Renu Laboratories, LLC; the most recent is dated Jul 27, 2022.
When was Renu Laboratories, LLC last inspected by FDA?
The most recent FDA inspection document on file for Renu Laboratories, LLC is a Form 483 dated Jul 27, 2022, for the site in Warminster, Pennsylvania.
What did FDA cite at Renu Laboratories, LLC?
The regulations cited most in the observations on file for Renu Laboratories, LLC are 21 CFR 211.111 (Time limitations on production), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.198(a) (Complaint files), 1 time.