Medefil Incorporated
FDA inspection history in Glendale Heights, Illinois, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Glendale Heights, Illinois.
Cited most
Across all Medefil Incorporated observations on file
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.80(a)General requirements1
- 21 CFR 211.94(c)Drug product containers and closures1
- 21 CFR 820.70(e)Production and process controls1
The complete Medefil Incorporated file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Glendale Heights, Illinois
One Form 483 · 2016 · 7 observations
Latest: Form 483, Jun 17, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-06-17 | 483 Form 483 | Glendale Heights, Illinois | 7 | $99 |
Investigators on these documents
FEI number 3001677091 · most recent document Jun 17, 2016
About Medefil Incorporated
How many FDA Form 483s has Medefil Incorporated received?
FDA Intel has 1 Form 483 on file for Medefil Incorporated; the most recent is dated Jun 17, 2016.
When was Medefil Incorporated last inspected by FDA?
The most recent FDA inspection document on file for Medefil Incorporated is a Form 483 dated Jun 17, 2016, for the site in Glendale Heights, Illinois.
What did FDA cite at Medefil Incorporated?
The regulations cited most in the observations on file for Medefil Incorporated are 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.80(a) (General requirements), 1 time.