Biosynergy, Inc
FDA inspection history in Elk Grove Village, Illinois, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Elk Grove Village, Illinois.
Cited most
Across all Biosynergy observations on file
- 21 CFR 820.198(a)Complaint files2
- 21 CFR 820.22Quality audit2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.70(c)Production and process controls1
- 21 CFR 820.90(a)Nonconforming product1
The complete Biosynergy file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Elk Grove Village, Illinois
One Form 483 · 2018 · 7 observations
Latest: Form 483, Jan 25, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-01-25 | 483 Form 483 | Elk Grove Village, Illinois | 7 | $99 |
Investigators on these documents
FEI number 1419300 · most recent document Jan 25, 2018
About Biosynergy, Inc
How many FDA Form 483s has Biosynergy, Inc received?
FDA Intel has 1 Form 483 on file for Biosynergy, Inc; the most recent is dated Jan 25, 2018.
When was Biosynergy, Inc last inspected by FDA?
The most recent FDA inspection document on file for Biosynergy, Inc is a Form 483 dated Jan 25, 2018, for the site in Elk Grove Village, Illinois.
What did FDA cite at Biosynergy, Inc?
The regulations cited most in the observations on file for Biosynergy, Inc are 21 CFR 820.198(a) (Complaint files), 2 times; 21 CFR 820.22 (Quality audit), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.