Orchid Detroit
FDA inspection history in Farmington Hills, Michigan, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Farmington Hills, Michigan.
Cited most
Across all Orchid Detroit observations on file
- 21 CFR 820.75Process validation1
- 21 CFR 820.90Nonconforming product1
The complete Orchid Detroit file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Farmington Hills, Michigan
One Form 483 · 2016 · 2 observations
Latest: Form 483, Mar 10, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-10 | 483 Form 483 | Farmington Hills, Michigan | 2 | $99 |
Investigators on these documents
FEI number 3011277306 · most recent document Mar 10, 2016
About Orchid Detroit
How many FDA Form 483s has Orchid Detroit received?
FDA Intel has 1 Form 483 on file for Orchid Detroit; the most recent is dated Mar 10, 2016.
When was Orchid Detroit last inspected by FDA?
The most recent FDA inspection document on file for Orchid Detroit is a Form 483 dated Mar 10, 2016, for the site in Farmington Hills, Michigan.
What did FDA cite at Orchid Detroit?
The regulations cited most in the observations on file for Orchid Detroit are 21 CFR 820.75 (Process validation), 1 time; 21 CFR 820.90 (Nonconforming product), 1 time.