Implant Direct Sybron Manufacturing LLC
FDA inspection history in Thousand Oaks, California, 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 Thousand Oaks, California.
Cited most
Across all Implant Direct Sybron Manufacturing observations on file
- 21 CFR 820.100(b)Corrective and preventive action1
The complete Implant Direct Sybron Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Thousand Oaks, California
One Form 483 · 2021 · 1 observation
Latest: Form 483, May 12, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-05-12 | 483 Form 483 | Thousand Oaks, California | 1 | $99 |
Investigators on these documents
FEI number 3001617766 · most recent document May 12, 2021
About Implant Direct Sybron Manufacturing LLC
How many FDA Form 483s has Implant Direct Sybron Manufacturing LLC received?
FDA Intel has 1 Form 483 on file for Implant Direct Sybron Manufacturing LLC; the most recent is dated May 12, 2021.
When was Implant Direct Sybron Manufacturing LLC last inspected by FDA?
The most recent FDA inspection document on file for Implant Direct Sybron Manufacturing LLC is a Form 483 dated May 12, 2021, for the site in Thousand Oaks, California.
What did FDA cite at Implant Direct Sybron Manufacturing LLC?
The regulations cited most in the observations on file for Implant Direct Sybron Manufacturing LLC are 21 CFR 820.100(b) (Corrective and preventive action), 1 time.