Tecomet, Inc
FDA inspection history in Pennsauken, New Jersey, 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 Pennsauken, New Jersey.
Cited most
Across all Tecomet observations on file
- 21 CFR 820.80(b)Receiving, in-process, and finished device acceptance3
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
The complete Tecomet file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pennsauken, New Jersey
One Form 483 · 2019 · 5 observations
Latest: Form 483, May 10, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-10 | 483 Form 483 | Pennsauken, New Jersey | 5 | $99 |
Investigators on these documents
FEI number 3011660613 · most recent document May 10, 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 May 10, 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 May 10, 2019, for the site in Pennsauken, New Jersey.
What did FDA cite at Tecomet, Inc?
The regulations cited most in the observations on file for Tecomet, Inc are 21 CFR 820.80(b) (Receiving, in-process, and finished device acceptance), 3 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.72(a) (Inspection, measuring, and test equipment), 1 time.