Tecomet, Inc.
FDA inspection history in Boulder, Colorado, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Boulder, Colorado.
Cited most
Across all Tecomet observations on file
- 21 CFR 820.75(a)Process validation1
The complete Tecomet file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Boulder, Colorado
One Form 483 · 2019 · 1 observation
Latest: Form 483, Nov 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-15 | 483 Form 483 | Boulder, Colorado | 1 | $99 |
Investigators on these documents
FEI number 3007137928 · most recent document Nov 15, 2019
About Tecomet, Inc.
How many FDA Form 483s has Tecomet, Inc. received?
FDA Intel has 1 Form 483 on file for Tecomet, Inc.; the most recent is dated Nov 15, 2019.
When was Tecomet, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Tecomet, Inc. is a Form 483 dated Nov 15, 2019, for the site in Boulder, Colorado.
What did FDA cite at Tecomet, Inc.?
The regulations cited most in the observations on file for Tecomet, Inc. are 21 CFR 820.75(a) (Process validation), 1 time.