Alick's Home Medical Equipment, Inc.
FDA inspection history in South Bend, Indiana, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at South Bend, Indiana.
Cited most
Across all Alick's Home Medical Equipment observations on file
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.198(b)Complaint files1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
- 21 CFR 211.80(a)General requirements1
The complete Alick's Home Medical Equipment file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
South Bend, Indiana
One Form 483 · 2021 · 5 observations
Latest: Form 483, Sep 3, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-09-03 | 483 Form 483 | South Bend, Indiana | 5 | $99 |
FEI number 1000115400 · most recent document Sep 3, 2021
About Alick's Home Medical Equipment, Inc.
How many FDA Form 483s has Alick's Home Medical Equipment, Inc. received?
FDA Intel has 1 Form 483 on file for Alick's Home Medical Equipment, Inc.; the most recent is dated Sep 3, 2021.
When was Alick's Home Medical Equipment, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Alick's Home Medical Equipment, Inc. is a Form 483 dated Sep 3, 2021, for the site in South Bend, Indiana.
What did FDA cite at Alick's Home Medical Equipment, Inc.?
The regulations cited most in the observations on file for Alick's Home Medical Equipment, Inc. are 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.198(b) (Complaint files), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.