Steritec Products Mfc. Co., Inc
FDA inspection history in Englewood, Colorado, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Englewood, Colorado.
Cited most
Across all Steritec Products Mfc. Co. observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
- 21 CFR 820.80(b)Receiving, in-process, and finished device acceptance1
The complete Steritec Products Mfc. Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Englewood, Colorado
One Form 483 · 2017 · 3 observations
Latest: Form 483, Feb 1, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-02-01 | 483 Form 483 | Englewood, Colorado | 3 | $99 |
Investigators on these documents
FEI number 1000125215 · most recent document Feb 1, 2017
About Steritec Products Mfc. Co., Inc
How many FDA Form 483s has Steritec Products Mfc. Co., Inc received?
FDA Intel has 1 Form 483 on file for Steritec Products Mfc. Co., Inc; the most recent is dated Feb 1, 2017.
When was Steritec Products Mfc. Co., Inc last inspected by FDA?
The most recent FDA inspection document on file for Steritec Products Mfc. Co., Inc is a Form 483 dated Feb 1, 2017, for the site in Englewood, Colorado.
What did FDA cite at Steritec Products Mfc. Co., Inc?
The regulations cited most in the observations on file for Steritec Products Mfc. Co., Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.72(a) (Inspection, measuring, and test equipment), 1 time; 21 CFR 820.80(b) (Receiving, in-process, and finished device acceptance), 1 time.