ASCLEMED USA INC. DBA ENOVACHEM
FDA inspection history in Torrance, California, 2018 to 2019
- 1
- Close-out
- 1
- Form 483
Every document, by year
- Close-out
- Form 483
2018: one Form 483; 2019: one close-out letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2018–19One Form 483 and one close-out letter, at Torrance, California.
Cited most
Across all ASCLEMED USA INC. DBA ENOVACHEM observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete ASCLEMED USA INC. DBA ENOVACHEM file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Torrance, California
One close-out letter and one Form 483 · 2018 to 2019 · 3 observations
Latest: Close-out, Jun 11, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-06-11 | Close-out Close-out letter | Torrance, California | — | $99 |
| 2018-09-27 | 483 Form 483 | Torrance, California | 3 | $99 |
Investigators on these documents
FEI number 3001452204 · most recent document Jun 11, 2019
About ASCLEMED USA INC. DBA ENOVACHEM
How many FDA Form 483s has ASCLEMED USA INC. DBA ENOVACHEM received?
FDA Intel has 1 Form 483 on file for ASCLEMED USA INC. DBA ENOVACHEM; the most recent is dated Sep 27, 2018.
When was ASCLEMED USA INC. DBA ENOVACHEM last inspected by FDA?
The most recent FDA inspection document on file for ASCLEMED USA INC. DBA ENOVACHEM is a Form 483 dated Sep 27, 2018, for the site in Torrance, California.
What did FDA cite at ASCLEMED USA INC. DBA ENOVACHEM?
The regulations cited most in the observations on file for ASCLEMED USA INC. DBA ENOVACHEM are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.